|
ENST00000524561.2:n.4201A>G
|
|
|
|
ENST00000526037.6:n.535A>G
|
|
|
|
ENST00000528374.2:c.1191A>G
|
|
|
|
ENST00000529967.6:n.2939A>G
|
|
|
|
ENST00000532220.2:n.3833A>G
|
|
|
|
ENST00000642611.2:n.5933A>G
|
|
|
|
ENST00000644057.2:n.1176A>G
|
|
|
|
ENST00000645004.2:n.2099A>G
|
|
|
|
ENST00000682051.1:n.4762A>G
|
|
|
|
ENST00000682110.1:n.4815A>G
|
|
|
|
ENST00000682140.1:c.*386A>G
|
ENSP00000507829.1:n.*386A>G
|
|
|
ENST00000682185.1:n.5905A>G
|
|
|
|
ENST00000682204.1:c.*2738A>G
|
ENSP00000507094.1:n.*2738A>G
|
|
|
ENST00000682215.1:n.5182A>G
|
|
|
|
ENST00000682288.1:c.*3031A>G
|
ENSP00000507506.1:n.*3031A>G
|
|
|
ENST00000682442.1:n.5035A>G
|
|
|
|
ENST00000682528.1:n.4892A>G
|
|
|
|
ENST00000682673.1:n.4759A>G
|
|
|
|
ENST00000682805.1:n.5220A>G
|
|
|
|
ENST00000682965.1:c.*1022A>G
|
ENSP00000508229.1:n.*1022A>G
|
|
|
ENST00000683093.1:n.5795A>G
|
|
|
|
ENST00000683136.1:c.4483A>G
|
ENSP00000507768.1:p.Thr1495Ala
|
|
|
ENST00000683153.1:n.4857A>G
|
|
|
|
ENST00000683365.1:n.4917A>G
|
|
|
|
ENST00000683377.1:n.4711A>G
|
|
|
|
ENST00000683456.1:c.*1737A>G
|
ENSP00000508318.1:n.*1737A>G
|
|
|
ENST00000683522.1:n.4897A>G
|
|
|
|
ENST00000683562.1:c.*2665A>G
|
ENSP00000508265.1:n.*2665A>G
|
|
|
ENST00000683693.1:n.6276A>G
|
|
|
|
ENST00000683725.1:c.*65A>G
|
ENSP00000507496.1:n.*65A>G
|
|
|
ENST00000684010.1:n.4810A>G
|
|
|
|
ENST00000684014.1:n.787A>G
|
|
|
|
ENST00000684157.1:n.5800A>G
|
|
|
|
ENST00000684253.1:n.4718A>G
|
|
|
|
ENST00000684288.1:c.*2772A>G
|
ENSP00000507143.1:n.*2772A>G
|
|
|
ENST00000684313.1:n.4247A>G
|
|
|
|
ENST00000684332.1:n.4888A>G
|
|
|
|
ENST00000684371.1:n.4921A>G
|
|
|
|
ENST00000684404.1:n.5843A>G
|
|
|
|
ENST00000684442.1:n.5039A>G
|
|
|
|
ENST00000684555.1:c.*2812A>G
|
ENSP00000507705.1:n.*2812A>G
|
|
|
ENST00000684571.1:c.4441A>G
|
ENSP00000506935.1:p.Thr1481Ala
|
|
|
ENST00000684593.1:c.*4305A>G
|
ENSP00000507005.1:n.*4305A>G
|
|
|
ENST00000684711.1:c.*2996A>G
|
ENSP00000506841.1:n.*2996A>G
|
|
|
ENST00000302539.9:c.4603A>G
|
ENSP00000303960.4:p.Thr1535Ala
|
|
|
ENST00000389817.8:c.4600A>G
MANE Select
|
ENSP00000374467.4:p.Thr1534Ala
|
|
|
ENST00000642271.1:c.4597A>G
|
ENSP00000493749.1:p.Thr1533Ala
|
|
|
ENST00000642579.1:c.2654A>G
|
|
|
|
ENST00000642611.1:n.5818A>G
|
|
|
|
ENST00000642902.1:c.4382A>G
|
|
|
|
ENST00000643260.1:c.4600A>G
|
ENSP00000494450.1:p.Thr1534Ala
|
|
|
ENST00000643562.1:c.*2722A>G
|
ENSP00000496124.1:n.*2722A>G
|
|
|
ENST00000643925.1:c.3185+561A>G
|
|
|
|
ENST00000644057.1:n.759A>G
|
|
|
|
ENST00000644484.1:c.*3986A>G
|
ENSP00000493558.1:n.*3986A>G
|
|
|
ENST00000644675.1:c.*2772A>G
|
ENSP00000494567.1:n.*2772A>G
|
|
|
ENST00000644757.1:c.*3203-725A>G
|
ENSP00000495085.1:n.*3203-725A>G
|
|
|
ENST00000644772.1:c.4666A>G
|
ENSP00000494321.1:p.Thr1556Ala
|
|
|
ENST00000645004.1:n.2293A>G
|
|
|
|
ENST00000645076.1:c.3695A>G
|
|
|
|
ENST00000645417.1:c.1788A>G
|
|
|
|
ENST00000645744.1:c.*4285A>G
|
ENSP00000494564.1:n.*4285A>G
|
|
|
ENST00000645760.1:c.5021A>G
|
|
|
|
ENST00000645884.1:c.*1883A>G
|
ENSP00000495516.1:n.*1883A>G
|
|
|
ENST00000646003.1:c.*2622A>G
|
ENSP00000495259.1:n.*2622A>G
|
|
|
ENST00000646207.1:c.*3437A>G
|
ENSP00000495025.1:n.*3437A>G
|
|
|
ENST00000646276.1:c.*4004A>G
|
ENSP00000496070.1:n.*4004A>G
|
|
|
ENST00000646592.1:c.3906A>G
|
|
|
|
ENST00000646902.1:c.4567A>G
|
ENSP00000494101.1:p.Thr1523Ala
|
|
|
ENST00000646993.1:c.*3038A>G
|
ENSP00000493720.1:n.*3038A>G
|
|
|
ENST00000647015.1:c.4351A>G
|
ENSP00000495389.1:p.Thr1451Ala
|
|
|
ENST00000647086.1:c.*4186A>G
|
ENSP00000493677.1:n.*4186A>G
|
|
|
ENST00000647158.1:c.*2887A>G
|
ENSP00000495744.1:n.*2887A>G
|
|
|
ENST00000302539.8:c.4603A>G
|
ENSP00000303960.4:p.Thr1535Ala
|
|
|
ENST00000389817.7:c.4600A>G
|
ENSP00000374467.3:p.Thr1534Ala
|
|
|
ENST00000525022.1:n.495A>G
|
|
|
|
ENST00000526037.5:n.360A>G
|
|
|
|
ENST00000526168.5:c.388A>G
|
|
|
|
ENST00000531642.5:c.631A>G
|
|
|
|
NM_000352.4:c.4600A>G
|
NP_000343.2:p.Thr1534Ala
|
|
|
NM_001287174.1:c.4603A>G
|
NP_001274103.1:p.Thr1535Ala
|
|
|
XM_011520331.1:c.4600A>G
|
XP_011518633.1:p.Thr1534Ala
|
|
|
XM_011520333.1:c.3100A>G
|
XP_011518635.1:p.Thr1034Ala
|
|
|
XR_930890.1:n.4562A>G
|
|
|
|
NM_001351295.1:c.4666A>G
|
NP_001338224.1:p.Thr1556Ala
|
|
|
NM_001351296.1:c.4600A>G
|
NP_001338225.1:p.Thr1534Ala
|
|
|
NM_001351297.1:c.4597A>G
|
NP_001338226.1:p.Thr1533Ala
|
|
|
NR_147094.1:n.4895A>G
|
|
|
|
XM_017018197.2:c.4669A>G
|
XP_016873686.1:p.Thr1557Ala
|
|
|
XM_017018199.1:c.4666A>G
|
XP_016873688.1:p.Thr1556Ala
|
|
|
XM_017018202.1:c.3166A>G
|
XP_016873691.1:p.Thr1056Ala
|
|
|
XM_017018204.1:c.2557A>G
|
XP_016873693.1:p.Thr853Ala
|
|
|
XM_024448668.1:c.2968A>G
|
XP_024304436.1:p.Thr990Ala
|
|
|
XR_001747945.2:n.4637A>G
|
|
|
|
XR_001747946.2:n.4568A>G
|
|
|
|
XR_002957189.1:n.6351A>G
|
|
|
|
NM_000352.6:c.4600A>G
MANE Select
|
NP_000343.2:p.Thr1534Ala
|
|
|
NM_001287174.2:c.4603A>G
|
NP_001274103.1:p.Thr1535Ala
|
|
|
NM_001351295.2:c.4666A>G
|
NP_001338224.1:p.Thr1556Ala
|
|
|
NM_001351296.2:c.4600A>G
|
NP_001338225.1:p.Thr1534Ala
|
|
|
NM_001351297.2:c.4597A>G
|
NP_001338226.1:p.Thr1533Ala
|
|
|
NR_147094.2:n.4895A>G
|
|
|
|
NM_001287174.3:c.4603A>G
|
NP_001274103.1:p.Thr1535Ala
|
|
