| 基因名 | 突变 |
|---|---|
| TTN(NM_001267550,titin,35991aa) | g.2:179436715G>A,c.74144C>T,p.P24715L |
| TTN(NM_001267550,titin,35991aa) | g.2:179436668C>T,c.74191G>A,p.E24731K |
| TTN(NM_001267550,titin,35991aa) | g.2:179436332T>C,c.74527A>G,p.N24843D |
| TTN(NM_001267550,titin,35991aa) | g.2:179436020G>A,c.74839C>T,p.R24947C |
| TTN(NM_001267550,titin,35991aa) | g.2:179435825G>A,c.75034C>T,p.R25012W |
| TTN(NM_001267550,titin,35991aa) | g.2:179435665T>C,c.75194A>G,p.H25065R |
| TTN(NM_001267550,titin,35991aa) | g.2:179435305T>G,c.75554A>C,p.K25185T |
| TTN(NM_001267550,titin,35991aa) | g.2:179434829G>A,c.76030C>T,p.R25344W |
| TTN(NM_001267550,titin,35991aa) | g.2:179434516C>T,c.76343G>A,p.S25448N |
| TTN(NM_001267550,titin,35991aa) | g.2:179434160C>A,c.76699G>T,p.V25567F |
| TTN(NM_001267550,titin,35991aa) | g.2:179434139A>G,c.76720T>C,p.Y25574H |
| TTN(NM_001267550,titin,35991aa) | g.2:179434121T>C,c.76738A>G,p.T25580A |
| TTN(NM_001267550,titin,35991aa) | g.2:179434120G>A,c.76739C>T,p.T25580M |
| TTN(NM_001267550,titin,35991aa) | g.2:179433872C>T,c.76987G>A,p.D25663N |
| TTN(NM_001267550,titin,35991aa) | g.2:179433580T>C,c.77279A>G,p.N25760S |
| TTN(NM_001267550,titin,35991aa) | g.2:179433221T>C,c.77638A>G,p.T25880A |
| TTN(NM_001267550,titin,35991aa) | g.2:179432185A>G,c.78674T>C,p.I26225T |
| TTN(NM_001267550,titin,35991aa) | g.2:179431633C>T,c.79226G>A,p.R26409H |
| TTN(NM_001267550,titin,35991aa) | g.2:179431594A>G,c.79265T>C,p.I26422T |
| TTN(NM_001267550,titin,35991aa) | g.2:179431540C>T,c.79319G>A,p.R26440H |
| TTN(NM_001267550,titin,35991aa) | g.2:179431159T>C,c.79700A>G,p.N26567S |
| TTN(NM_001267550,titin,35991aa) | g.2:179431076C>G,c.79783G>C,p.D26595H |
| TTN(NM_001267550,titin,35991aa) | g.2:179430997G>A,c.79862C>T,p.T26621M |
| TTN(NM_001267550,titin,35991aa) | g.2:179430631T>G,c.80228A>C,p.K26743T |
| TTN(NM_001267550,titin,35991aa) | g.2:179430001G>A,c.80858C>T,p.T26953M |
| TTN(NM_001267550,titin,35991aa) | g.2:179429954C>T,c.80905G>A,p.V26969I |
| TTN(NM_001267550,titin,35991aa) | g.2:179429915A>G,c.80944T>C,p.F26982L |
| TTN(NM_001267550,titin,35991aa) | g.2:179429821C>T,c.81038G>A,p.R27013Q |