| 基因名 | 突变 |
|---|---|
| TTN(NM_001267550,titin,35991aa) | g.2:179498717A>G,c.42509T>C,p.M14170T |
| TTN(NM_001267550,titin,35991aa) | g.2:179498042T>C,c.42958A>G,p.K14320E |
| TTN(NM_001267550,titin,35991aa) | g.2:179497056T>C,c.43565A>G,p.H14522R |
| TTN(NM_001267550,titin,35991aa) | g.2:179496930G>C,c.43691C>G,p.S14564C |
| TTN(NM_001267550,titin,35991aa) | g.2:179494029T>G,c.44423A>C,p.K14808T |
| TTN(NM_001267550,titin,35991aa) | g.2:179486648T>G,c.45001A>C,p.N15001H |
| TTN(NM_001267550,titin,35991aa) | g.2:179486431A>C,c.45120T>G,p.I15040M |
| TTN(NM_001267550,titin,35991aa) | g.2:179486376C>T,c.45175G>A,p.A15059T |
| TTN(NM_001267550,titin,35991aa) | g.2:179486339A>G,c.45212T>C,p.I15071T |
| TTN(NM_001267550,titin,35991aa) | g.2:179486223C>T,c.45328G>A,p.D15110N |
| TTN(NM_001267550,titin,35991aa) | g.2:179486037C>A,c.45408G>T,p.K15136N |
| TTN(NM_001267550,titin,35991aa) | g.2:179485612C>T,c.45725G>A,p.R15242K |
| TTN(NM_001267550,titin,35991aa) | g.2:179485269G>A,c.45979C>T,p.R15327C |
| TTN(NM_001267550,titin,35991aa) | g.2:179485268C>T,c.45980G>A,p.R15327H |
| TTN(NM_001267550,titin,35991aa) | g.2:179485106A>G,c.46142T>C,p.V15381A |
| TTN(NM_001267550,titin,35991aa) | g.2:179485028T>C,c.46220A>G,p.D15407G |
| TTN(NM_001267550,titin,35991aa) | g.2:179484555C>A,c.46489G>T,p.V15497F |
| TTN(NM_001267550,titin,35991aa) | g.2:179483430G>A,c.46847C>T,p.T15616M |
| TTN(NM_001267550,titin,35991aa) | g.2:179483108C>T,c.47077G>A,p.V15693I |
| TTN(NM_001267550,titin,35991aa) | g.2:179482987C>T,c.47198G>A,p.S15733N |
| TTN(NM_001267550,titin,35991aa) | g.2:179482937C>T,c.47248G>A,p.V15750I |
| TTN(NM_001267550,titin,35991aa) | g.2:179482800C>T,c.47278G>A,p.G15760S |
| TTN(NM_001267550,titin,35991aa) | g.2:179482763C>T,c.47315G>A,p.R15772Q |
| TTN(NM_001267550,titin,35991aa) | g.2:179482533G>T,c.47545C>A,p.P15849T |
| TTN(NM_001267550,titin,35991aa) | g.2:179482119C>T,c.47693G>A,p.R15898Q |
| TTN(NM_001267550,titin,35991aa) | g.2:179482089C>T,c.47723G>A,p.R15908H |
| TTN(NM_001267550,titin,35991aa) | g.2:179481955C>T,c.47767G>A,p.G15923R |
| TTN(NM_001267550,titin,35991aa) | g.2:179481862C>T,c.47860G>A,p.A15954T |