|
ENST00000524561.2:n.4045A>T
|
|
|
|
ENST00000526037.6:n.379A>T
|
|
|
|
ENST00000528374.2:c.1035A>T
|
|
|
|
ENST00000529967.6:n.2783A>T
|
|
|
|
ENST00000532220.2:n.3677A>T
|
|
|
|
ENST00000642611.2:n.5777A>T
|
|
|
|
ENST00000644057.2:n.1020A>T
|
|
|
|
ENST00000645004.2:n.1943A>T
|
|
|
|
ENST00000682051.1:n.4606A>T
|
|
|
|
ENST00000682110.1:n.4659A>T
|
|
|
|
ENST00000682140.1:c.*230A>T
|
ENSP00000507829.1:n.*230A>T
|
|
|
ENST00000682185.1:n.5749A>T
|
|
|
|
ENST00000682204.1:c.*2582A>T
|
ENSP00000507094.1:n.*2582A>T
|
|
|
ENST00000682215.1:n.5026A>T
|
|
|
|
ENST00000682288.1:c.*2875A>T
|
ENSP00000507506.1:n.*2875A>T
|
|
|
ENST00000682442.1:n.4879A>T
|
|
|
|
ENST00000682528.1:n.4736A>T
|
|
|
|
ENST00000682673.1:n.4603A>T
|
|
|
|
ENST00000682805.1:n.5064A>T
|
|
|
|
ENST00000682965.1:c.*866A>T
|
ENSP00000508229.1:n.*866A>T
|
|
|
ENST00000683093.1:n.5639A>T
|
|
|
|
ENST00000683136.1:c.4327A>T
|
ENSP00000507768.1:p.Ser1443Cys
|
|
|
ENST00000683153.1:n.4701A>T
|
|
|
|
ENST00000683365.1:n.4761A>T
|
|
|
|
ENST00000683377.1:n.4555A>T
|
|
|
|
ENST00000683456.1:c.*1581A>T
|
ENSP00000508318.1:n.*1581A>T
|
|
|
ENST00000683522.1:n.4741A>T
|
|
|
|
ENST00000683562.1:c.*2509A>T
|
ENSP00000508265.1:n.*2509A>T
|
|
|
ENST00000683693.1:n.6120A>T
|
|
|
|
ENST00000683725.1:c.4340A>T
|
ENSP00000507496.1:p.Gln1447Leu
|
|
|
ENST00000684010.1:n.4654A>T
|
|
|
|
ENST00000684014.1:n.631A>T
|
|
|
|
ENST00000684157.1:n.5644A>T
|
|
|
|
ENST00000684253.1:n.4562A>T
|
|
|
|
ENST00000684288.1:c.*2616A>T
|
ENSP00000507143.1:n.*2616A>T
|
|
|
ENST00000684313.1:n.4091A>T
|
|
|
|
ENST00000684332.1:n.4732A>T
|
|
|
|
ENST00000684371.1:n.4765A>T
|
|
|
|
ENST00000684404.1:n.5687A>T
|
|
|
|
ENST00000684442.1:n.4883A>T
|
|
|
|
ENST00000684555.1:c.*2656A>T
|
ENSP00000507705.1:n.*2656A>T
|
|
|
ENST00000684571.1:c.4285A>T
|
ENSP00000506935.1:p.Ser1429Cys
|
|
|
ENST00000684593.1:c.*4149A>T
|
ENSP00000507005.1:n.*4149A>T
|
|
|
ENST00000684711.1:c.*2840A>T
|
ENSP00000506841.1:n.*2840A>T
|
|
|
ENST00000302539.9:c.4447A>T
|
ENSP00000303960.4:p.Ser1483Cys
|
|
|
ENST00000389817.8:c.4444A>T
MANE Select
|
ENSP00000374467.4:p.Ser1482Cys
|
|
|
ENST00000642271.1:c.4441A>T
|
ENSP00000493749.1:p.Ser1481Cys
|
|
|
ENST00000642579.1:c.2498A>T
|
|
|
|
ENST00000642611.1:n.5662A>T
|
|
|
|
ENST00000642902.1:c.4226A>T
|
|
|
|
ENST00000643260.1:c.4444A>T
|
ENSP00000494450.1:p.Ser1482Cys
|
|
|
ENST00000643562.1:c.*2566A>T
|
ENSP00000496124.1:n.*2566A>T
|
|
|
ENST00000643925.1:c.3084A>T
|
|
|
|
ENST00000644057.1:n.603A>T
|
|
|
|
ENST00000644484.1:c.*3830A>T
|
ENSP00000493558.1:n.*3830A>T
|
|
|
ENST00000644675.1:c.*2616A>T
|
ENSP00000494567.1:n.*2616A>T
|
|
|
ENST00000644757.1:c.*3203-1387A>T
|
ENSP00000495085.1:n.*3203-1387A>T
|
|
|
ENST00000644772.1:c.4510A>T
|
ENSP00000494321.1:p.Ser1504Cys
|
|
|
ENST00000645004.1:n.2137A>T
|
|
|
|
ENST00000645076.1:c.3539A>T
|
|
|
|
ENST00000645417.1:c.1632A>T
|
|
|
|
ENST00000645744.1:c.*4129A>T
|
ENSP00000494564.1:n.*4129A>T
|
|
|
ENST00000645760.1:c.4865A>T
|
|
|
|
ENST00000645884.1:c.*1727A>T
|
ENSP00000495516.1:n.*1727A>T
|
|
|
ENST00000646003.1:c.*2466A>T
|
ENSP00000495259.1:n.*2466A>T
|
|
|
ENST00000646207.1:c.*3281A>T
|
ENSP00000495025.1:n.*3281A>T
|
|
|
ENST00000646276.1:c.*3848A>T
|
ENSP00000496070.1:n.*3848A>T
|
|
|
ENST00000646592.1:c.3750A>T
|
|
|
|
ENST00000646902.1:c.4411A>T
|
ENSP00000494101.1:p.Ser1471Cys
|
|
|
ENST00000646993.1:c.*2882A>T
|
ENSP00000493720.1:n.*2882A>T
|
|
|
ENST00000647013.1:c.4450A>T
|
ENSP00000496741.1:n.4450A>T
|
|
|
ENST00000647015.1:c.4195A>T
|
ENSP00000495389.1:p.Ser1399Cys
|
|
|
ENST00000647086.1:c.*4030A>T
|
ENSP00000493677.1:n.*4030A>T
|
|
|
ENST00000647158.1:c.*2731A>T
|
ENSP00000495744.1:n.*2731A>T
|
|
|
ENST00000302539.8:c.4447A>T
|
ENSP00000303960.4:p.Ser1483Cys
|
|
|
ENST00000389817.7:c.4444A>T
|
ENSP00000374467.3:p.Ser1482Cys
|
|
|
ENST00000525022.1:n.339A>T
|
|
|
|
ENST00000526037.5:n.204A>T
|
|
|
|
ENST00000526168.5:c.232A>T
|
|
|
|
ENST00000531642.5:c.475A>T
|
|
|
|
NM_000352.4:c.4444A>T
|
NP_000343.2:p.Ser1482Cys
|
|
|
NM_001287174.1:c.4447A>T
|
NP_001274103.1:p.Ser1483Cys
|
|
|
XM_011520331.1:c.4444A>T
|
XP_011518633.1:p.Ser1482Cys
|
|
|
XM_011520332.1:c.4343A>T
|
XP_011518634.1:p.Gln1448Leu
|
|
|
XM_011520333.1:c.2944A>T
|
XP_011518635.1:p.Ser982Cys
|
|
|
XR_930890.1:n.4406A>T
|
|
|
|
NM_001351295.1:c.4510A>T
|
NP_001338224.1:p.Ser1504Cys
|
|
|
NM_001351296.1:c.4444A>T
|
NP_001338225.1:p.Ser1482Cys
|
|
|
NM_001351297.1:c.4441A>T
|
NP_001338226.1:p.Ser1481Cys
|
|
|
NR_147094.1:n.4739A>T
|
|
|
|
XM_017018197.2:c.4513A>T
|
XP_016873686.1:p.Ser1505Cys
|
|
|
XM_017018199.1:c.4510A>T
|
XP_016873688.1:p.Ser1504Cys
|
|
|
XM_017018201.2:c.4409A>T
|
XP_016873690.1:p.Gln1470Leu
|
|
|
XM_017018202.1:c.3010A>T
|
XP_016873691.1:p.Ser1004Cys
|
|
|
XM_017018204.1:c.2401A>T
|
XP_016873693.1:p.Ser801Cys
|
|
|
XM_024448668.1:c.2812A>T
|
XP_024304436.1:p.Ser938Cys
|
|
|
XR_001747945.2:n.4481A>T
|
|
|
|
XR_001747946.2:n.4412A>T
|
|
|
|
XR_002957189.1:n.6195A>T
|
|
|
|
NM_000352.6:c.4444A>T
MANE Select
|
NP_000343.2:p.Ser1482Cys
|
|
|
NM_001287174.2:c.4447A>T
|
NP_001274103.1:p.Ser1483Cys
|
|
|
NM_001351295.2:c.4510A>T
|
NP_001338224.1:p.Ser1504Cys
|
|
|
NM_001351296.2:c.4444A>T
|
NP_001338225.1:p.Ser1482Cys
|
|
|
NM_001351297.2:c.4441A>T
|
NP_001338226.1:p.Ser1481Cys
|
|
|
NR_147094.2:n.4739A>T
|
|
|
|
NM_001287174.3:c.4447A>T
|
NP_001274103.1:p.Ser1483Cys
|
|
