| 基因名 | 突变 |
|---|---|
| TTN(NM_001267550,titin,35991aa) | g.2:179453729C>T,c.62723G>A,p.R20908Q |
| TTN(NM_001267550,titin,35991aa) | g.2:179453429G>A,c.63023C>T,p.T21008I |
| TTN(NM_001267550,titin,35991aa) | g.2:179453379C>T,c.63073G>A,p.V21025I |
| TTN(NM_001267550,titin,35991aa) | g.2:179452782G>A,c.63352C>T,p.R21118W |
| TTN(NM_001267550,titin,35991aa) | g.2:179452695C>T,c.63439G>A,p.A21147T |
| TTN(NM_001267550,titin,35991aa) | g.2:179452410C>T,c.63626G>A,p.R21209Q |
| TTN(NM_001267550,titin,35991aa) | g.2:179452261C>T,c.63775G>A,p.V21259I |
| TTN(NM_001267550,titin,35991aa) | g.2:179452031C>T,c.63907G>A,p.V21303M |
| TTN(NM_001267550,titin,35991aa) | g.2:179452021C>T,c.63917G>A,p.R21306H |
| TTN(NM_001267550,titin,35991aa) | g.2:179451454G>A,c.64174C>T,p.R21392C |
| TTN(NM_001267550,titin,35991aa) | g.2:179451420G>A,c.64208C>T,p.T21403I |
| TTN(NM_001267550,titin,35991aa) | g.2:179449687C>T,c.64681G>A,p.G21561S |
| TTN(NM_001267550,titin,35991aa) | g.2:179449579C>T,c.64789G>A,p.V21597M |
| TTN(NM_001267550,titin,35991aa) | g.2:179449557C>T,c.64811G>A,p.R21604Q |
| TTN(NM_001267550,titin,35991aa) | g.2:179449465G>A,c.64903C>T,p.R21635C |
| TTN(NM_001267550,titin,35991aa) | g.2:179449186G>A,c.65092C>T,p.R21698C |
| TTN(NM_001267550,titin,35991aa) | g.2:179449131G>A,c.65147C>T,p.S21716L |
| TTN(NM_001267550,titin,35991aa) | g.2:179448375G>A,c.65534C>T,p.P21845L |
| TTN(NM_001267550,titin,35991aa) | g.2:179447801A>G,c.65729T>C,p.I21910T |
| TTN(NM_001267550,titin,35991aa) | g.2:179447268C>T,c.65915G>A,p.R21972H |
| TTN(NM_001267550,titin,35991aa) | g.2:179447263T>C,c.65920A>G,p.M21974V |
| TTN(NM_001267550,titin,35991aa) | g.2:179446666C>T,c.66430G>A,p.A22144T |
| TTN(NM_001267550,titin,35991aa) | g.2:179446405C>T,c.66590G>A,p.R22197Q |
| TTN(NM_001267550,titin,35991aa) | g.2:179446381C>T,c.66614G>A,p.R22205K |
| TTN(NM_001267550,titin,35991aa) | g.2:179444939C>T,c.67075G>A,p.V22359I |
| TTN(NM_001267550,titin,35991aa) | g.2:179444768C>G,c.67246G>C,p.A22416P |
| TTN(NM_001267550,titin,35991aa) | g.2:179442792C>T,c.68450G>A,p.R22817Q |
| TTN(NM_001267550,titin,35991aa) | g.2:179442784C>G,c.68458G>C,p.A22820P |