| 基因名 | 突变 |
|---|---|
| TTN(NM_001267550,titin,35991aa) | g.2:179422801C>T,c.87280G>A,p.E29094K |
| TTN(NM_001267550,titin,35991aa) | g.2:179422669G>T,c.87412C>A,p.P29138T |
| TTN(NM_001267550,titin,35991aa) | g.2:179422181C>T,c.87808G>A,p.V29270I |
| TTN(NM_001267550,titin,35991aa) | g.2:179422112G>A,c.87877C>T,p.R29293C |
| TTN(NM_001267550,titin,35991aa) | g.2:179421775C>A,c.88106G>T,p.G29369V |
| TTN(NM_001267550,titin,35991aa) | g.2:179421758G>A,c.88123C>T,p.R29375C |
| TTN(NM_001267550,titin,35991aa) | g.2:179421698A>G,c.88183T>C,p.F29395L |
| TTN(NM_001267550,titin,35991aa) | g.2:179421694A>G,c.88187T>C,p.I29396T |
| TTN(NM_001267550,titin,35991aa) | g.2:179419792G>A,c.88394C>T,p.S29465F |
| TTN(NM_001267550,titin,35991aa) | g.2:179419676C>T,c.88510G>A,p.D29504N |
| TTN(NM_001267550,titin,35991aa) | g.2:179419341C>T,c.88733G>A,p.R29578H |
| TTN(NM_001267550,titin,35991aa) | g.2:179418854C>T,c.88984G>A,p.G29662S |
| TTN(NM_001267550,titin,35991aa) | g.2:179418772C>T,c.89066G>A,p.R29689H |
| TTN(NM_001267550,titin,35991aa) | g.2:179418492G>C,c.89240C>G,p.T29747S |
| TTN(NM_001267550,titin,35991aa) | g.2:179418346C>T,c.89386G>A,p.V29796M |
| TTN(NM_001267550,titin,35991aa) | g.2:179418306C>T,c.89426G>A,p.R29809Q |
| TTN(NM_001267550,titin,35991aa) | g.2:179417638A>T,c.89989T>A,p.L29997M |
| TTN(NM_001267550,titin,35991aa) | g.2:179417091C>T,c.90536G>A,p.R30179H |
| TTN(NM_001267550,titin,35991aa) | g.2:179416989A>G,c.90638T>C,p.I30213T |
| TTN(NM_001267550,titin,35991aa) | g.2:179416834G>A,c.90793C>T,p.R30265W |
| TTN(NM_001267550,titin,35991aa) | g.2:179416801A>C,c.90826T>G,p.C30276G |
| TTN(NM_001267550,titin,35991aa) | g.2:179416659C>T,c.90968G>A,p.R30323K |
| TTN(NM_001267550,titin,35991aa) | g.2:179414992T>C,c.91573A>G,p.I30525V |
| TTN(NM_001267550,titin,35991aa) | g.2:179414944C>T,c.91621G>A,p.G30541R |
| TTN(NM_001267550,titin,35991aa) | g.2:179414800C>T,c.91765G>A,p.A30589T |
| TTN(NM_001267550,titin,35991aa) | g.2:179414512T>C,c.91937A>G,p.N30646S |
| TTN(NM_001267550,titin,35991aa) | g.2:179414440A>G,c.92009T>C,p.I30670T |
| TTN(NM_001267550,titin,35991aa) | g.2:179414318C>T,c.92131G>A,p.V30711M |