ENST00000510830.2:n.1209T>C
|
|
|
ENST00000651892.2:c.8210T>C
MANE Select
|
ENSP00000498265.2:p.Val2737Ala
|
|
ENST00000425232.6:c.8048T>C
|
ENSP00000389014.2:p.Val2683Ala
|
|
ENST00000508244.5:c.8048T>C
|
ENSP00000421690.1:p.Val2683Ala
|
|
ENST00000509849.5:c.5222T>C
|
ENSP00000426337.1:p.Val1741Ala
|
|
ENST00000509957.5:n.452T>C
|
|
|
ENST00000511210.5:n.501T>C
|
|
|
ENST00000511824.2:c.1324T>C
|
|
|
ENST00000514429.5:c.5246T>C
|
ENSP00000424223.1:p.Val1749Ala
|
|
NM_023073.3:c.8048T>C
|
NP_075561.3:p.Val2683Ala
|
|
XM_005248345.2:c.8210T>C
|
XP_005248402.1:p.Val2737Ala
|
|
XM_005248346.2:c.8207T>C
|
XP_005248403.1:p.Val2736Ala
|
|
XM_005248347.2:c.8207T>C
|
XP_005248404.1:p.Val2736Ala
|
|
XM_005248349.2:c.8099T>C
|
XP_005248406.1:p.Val2700Ala
|
|
XM_005248350.2:c.8081T>C
|
XP_005248407.1:p.Val2694Ala
|
|
XM_005248353.3:c.4853T>C
|
XP_005248410.1:p.Val1618Ala
|
|
XM_006714489.2:c.8210T>C
|
XP_006714552.1:p.Val2737Ala
|
|
XM_006714491.2:c.2783T>C
|
XP_006714554.1:p.Val928Ala
|
|
XM_011514085.1:c.8210T>C
|
XP_011512387.1:p.Val2737Ala
|
|
XM_011514086.1:c.8210T>C
|
XP_011512388.1:p.Val2737Ala
|
|
XM_011514087.1:c.8156T>C
|
XP_011512389.1:p.Val2719Ala
|
|
XM_011514088.1:c.8102T>C
|
XP_011512390.1:p.Val2701Ala
|
|
XM_011514089.1:c.8210T>C
|
XP_011512391.1:p.Val2737Ala
|
|
XM_011514090.1:c.7892T>C
|
XP_011512392.1:p.Val2631Ala
|
|
XM_011514091.1:c.7538T>C
|
XP_011512393.1:p.Val2513Ala
|
|
XM_011514092.1:c.8210T>C
|
XP_011512394.1:p.Val2737Ala
|
|
XM_011514094.1:c.5435T>C
|
XP_011512396.1:p.Val1812Ala
|
|
XR_427661.2:n.8385T>C
|
|
|
XR_925644.1:n.8385T>C
|
|
|
XM_005248345.4:c.8210T>C
|
XP_005248402.1:p.Val2737Ala
|
|
XM_005248346.4:c.8207T>C
|
XP_005248403.1:p.Val2736Ala
|
|
XM_005248347.4:c.8207T>C
|
XP_005248404.1:p.Val2736Ala
|
|
XM_005248349.4:c.8099T>C
|
XP_005248406.1:p.Val2700Ala
|
|
XM_005248350.4:c.8081T>C
|
XP_005248407.1:p.Val2694Ala
|
|
XM_006714491.3:c.2783T>C
|
XP_006714554.1:p.Val928Ala
|
|
XM_011514085.3:c.8210T>C
|
XP_011512387.1:p.Val2737Ala
|
|
XM_011514086.3:c.8210T>C
|
XP_011512388.1:p.Val2737Ala
|
|
XM_011514087.2:c.8156T>C
|
XP_011512389.1:p.Val2719Ala
|
|
XM_011514088.2:c.8102T>C
|
XP_011512390.1:p.Val2701Ala
|
|
XM_011514089.2:c.8210T>C
|
XP_011512391.1:p.Val2737Ala
|
|
XM_011514090.3:c.7892T>C
|
XP_011512392.1:p.Val2631Ala
|
|
XM_011514092.2:c.8210T>C
|
XP_011512394.1:p.Val2737Ala
|
|
XM_011514094.2:c.5435T>C
|
XP_011512396.1:p.Val1812Ala
|
|
XM_017009760.1:c.8021T>C
|
XP_016865249.1:p.Val2674Ala
|
|
XM_017009761.2:c.8021T>C
|
XP_016865250.1:p.Val2674Ala
|
|
XM_017009763.1:c.7217T>C
|
XP_016865252.1:p.Val2406Ala
|
|
XM_017009765.1:c.7022T>C
|
XP_016865254.1:p.Val2341Ala
|
|
XM_017009766.1:c.4853T>C
|
XP_016865255.1:p.Val1618Ala
|
|
XM_024446183.1:c.8021T>C
|
XP_024301951.1:p.Val2674Ala
|
|
XM_024446184.1:c.7892T>C
|
XP_024301952.1:p.Val2631Ala
|
|
XM_024446185.1:c.7538T>C
|
XP_024301953.1:p.Val2513Ala
|
|
XM_024446186.1:c.7217T>C
|
XP_024301954.1:p.Val2406Ala
|
|
XR_001742208.1:n.8379T>C
|
|
|
XR_002956171.1:n.8325T>C
|
|
|
XR_925644.2:n.8434T>C
|
|
|
NM_001384732.1:c.8210T>C
MANE Select
|
NP_001371661.1:p.Val2737Ala
|
|
NM_023073.4:c.8048T>C
|
NP_075561.3:p.Val2683Ala
|
|