|
ENST00000371375.2:n.4251T>G
|
ENSP00000360426.1:p.Cys1417Trp
|
|
|
ENST00000685253.1:c.*1718T>G
|
ENSP00000509405.1:n.*1718T>G
|
|
|
ENST00000685889.1:n.1910T>G
|
|
|
|
ENST00000686807.1:n.594T>G
|
|
|
|
ENST00000686954.1:c.*459T>G
|
ENSP00000508416.1:n.*459T>G
|
|
|
ENST00000688810.1:n.4203T>G
|
ENSP00000509140.1:p.Cys1401Trp
|
|
|
ENST00000689233.1:n.9383T>G
|
|
|
|
ENST00000690340.1:n.2848T>G
|
|
|
|
ENST00000692286.1:c.5043T>G
|
ENSP00000509490.1:p.Cys1681Trp
|
|
|
ENST00000692396.1:c.5127T>G
|
ENSP00000508605.1:p.Cys1709Trp
|
|
|
ENST00000371380.8:c.5175T>G
MANE Select
|
ENSP00000360431.2:p.Cys1725Trp
|
|
|
ENST00000371385.8:c.4149T>G
|
ENSP00000360438.4:p.Cys1383Trp
|
|
|
ENST00000674738.1:n.3730T>G
|
|
|
|
ENST00000674827.1:n.3291T>G
|
ENSP00000502523.1:p.Cys1097Trp
|
|
|
ENST00000675218.1:n.4251T>G
|
ENSP00000501910.1:p.Cys1417Trp
|
|
|
ENST00000675487.1:c.*1108T>G
|
ENSP00000502340.1:n.*1108T>G
|
|
|
ENST00000675718.1:n.4444T>G
|
|
|
|
ENST00000676102.1:c.4020T>G
|
ENSP00000502811.1:p.Cys1340Trp
|
|
|
ENST00000260766.7:c.5175T>G
|
ENSP00000260766.3:p.Cys1725Trp
|
|
|
ENST00000371375.1:n.4251T>G
|
ENSP00000360426.1:p.Cys1417Trp
|
|
|
ENST00000371380.7:c.5175T>G
|
ENSP00000360431.2:p.Cys1725Trp
|
|
|
ENST00000371385.7:c.4251T>G
|
ENSP00000360438.3:p.Cys1417Trp
|
|
|
NM_001165979.2:c.4251T>G
|
NP_001159451.1:p.Cys1417Trp
|
|
|
NM_001288989.1:c.5127T>G
|
NP_001275918.1:p.Cys1709Trp
|
|
|
NM_016341.3:c.5175T>G
|
NP_057425.3:p.Cys1725Trp
|
|
|
XM_006717885.2:c.5217T>G
|
XP_006717948.1:p.Cys1739Trp
|
|
|
XM_006717886.2:c.5217T>G
|
XP_006717949.1:p.Cys1739Trp
|
|
|
XM_006717888.2:c.5214T>G
|
XP_006717951.1:p.Cys1738Trp
|
|
|
XM_006717889.2:c.5169T>G
|
XP_006717952.1:p.Cys1723Trp
|
|
|
XM_006717890.1:c.4293T>G
|
XP_006717953.1:p.Cys1431Trp
|
|
|
XM_011539849.1:c.5217T>G
|
XP_011538151.1:p.Cys1739Trp
|
|
|
XM_011539850.1:c.4062T>G
|
XP_011538152.1:p.Cys1354Trp
|
|
|
XM_006717885.4:c.5217T>G
|
XP_006717948.1:p.Cys1739Trp
|
|
|
XM_006717888.4:c.5214T>G
|
XP_006717951.1:p.Cys1738Trp
|
|
|
XM_006717889.4:c.5169T>G
|
XP_006717952.1:p.Cys1723Trp
|
|
|
XM_006717890.3:c.4293T>G
|
XP_006717953.1:p.Cys1431Trp
|
|
|
XM_011539849.3:c.5217T>G
|
XP_011538151.1:p.Cys1739Trp
|
|
|
XM_011539850.3:c.4062T>G
|
XP_011538152.1:p.Cys1354Trp
|
|
|
XM_017016310.2:c.5217T>G
|
XP_016871799.1:p.Cys1739Trp
|
|
|
XM_017016311.2:c.5217T>G
|
XP_016871800.1:p.Cys1739Trp
|
|
|
XM_017016312.2:c.4203T>G
|
XP_016871801.1:p.Cys1401Trp
|
|
|
NM_001288989.2:c.5127T>G
|
NP_001275918.1:p.Cys1709Trp
|
|
|
NM_016341.4:c.5175T>G
MANE Select
|
NP_057425.3:p.Cys1725Trp
|
|
