|
ENST00000524561.2:n.2975C>G
|
|
|
|
ENST00000529967.6:n.1745C>G
|
|
|
|
ENST00000532220.2:n.1138C>G
|
|
|
|
ENST00000642611.2:n.3475C>G
|
|
|
|
ENST00000645004.2:n.905C>G
|
|
|
|
ENST00000682051.1:n.3422C>G
|
|
|
|
ENST00000682110.1:n.3475C>G
|
|
|
|
ENST00000682140.1:c.3403C>G
|
ENSP00000507829.1:p.Pro1135Ala
|
|
|
ENST00000682185.1:n.4711C>G
|
|
|
|
ENST00000682204.1:c.*1544C>G
|
ENSP00000507094.1:n.*1544C>G
|
|
|
ENST00000682215.1:n.3472C>G
|
|
|
|
ENST00000682288.1:c.*1837C>G
|
ENSP00000507506.1:n.*1837C>G
|
|
|
ENST00000682442.1:n.3695C>G
|
|
|
|
ENST00000682528.1:n.3552C>G
|
|
|
|
ENST00000682673.1:n.3419C>G
|
|
|
|
ENST00000682805.1:n.3472C>G
|
|
|
|
ENST00000682965.1:c.3396+831C>G
|
ENSP00000508229.1:n.3396+831C>G
|
|
|
ENST00000683093.1:n.3574C>G
|
|
|
|
ENST00000683136.1:c.3403C>G
|
ENSP00000507768.1:p.Pro1135Ala
|
|
|
ENST00000683153.1:n.3631C>G
|
|
|
|
ENST00000683365.1:n.3577C>G
|
|
|
|
ENST00000683377.1:n.3475C>G
|
|
|
|
ENST00000683456.1:c.*543C>G
|
ENSP00000508318.1:n.*543C>G
|
|
|
ENST00000683522.1:n.3475C>G
|
|
|
|
ENST00000683562.1:c.*1575C>G
|
ENSP00000508265.1:n.*1575C>G
|
|
|
ENST00000683693.1:n.3552C>G
|
|
|
|
ENST00000683725.1:c.3406C>G
|
ENSP00000507496.1:p.Pro1136Ala
|
|
|
ENST00000684010.1:n.3470C>G
|
|
|
|
ENST00000684157.1:n.3475C>G
|
|
|
|
ENST00000684253.1:n.3378C>G
|
|
|
|
ENST00000684288.1:c.*1578C>G
|
ENSP00000507143.1:n.*1578C>G
|
|
|
ENST00000684313.1:n.2907C>G
|
|
|
|
ENST00000684332.1:n.3548C>G
|
|
|
|
ENST00000684371.1:n.3581C>G
|
|
|
|
ENST00000684404.1:n.3518C>G
|
|
|
|
ENST00000684442.1:n.3475C>G
|
|
|
|
ENST00000684555.1:c.*1618C>G
|
ENSP00000507705.1:n.*1618C>G
|
|
|
ENST00000684571.1:c.3247C>G
|
ENSP00000506935.1:p.Pro1083Ala
|
|
|
ENST00000684593.1:c.*3111C>G
|
ENSP00000507005.1:n.*3111C>G
|
|
|
ENST00000684711.1:c.*1802C>G
|
ENSP00000506841.1:n.*1802C>G
|
|
|
ENST00000302539.9:c.3409C>G
|
ENSP00000303960.4:p.Pro1137Ala
|
|
|
ENST00000389817.8:c.3406C>G
MANE Select
|
ENSP00000374467.4:p.Pro1136Ala
|
|
|
ENST00000642271.1:c.3403C>G
|
ENSP00000493749.1:p.Pro1135Ala
|
|
|
ENST00000642579.1:c.1490C>G
|
|
|
|
ENST00000642611.1:n.3360C>G
|
|
|
|
ENST00000642902.1:c.3188C>G
|
|
|
|
ENST00000643260.1:c.3406C>G
|
ENSP00000494450.1:p.Pro1136Ala
|
|
|
ENST00000643562.1:c.*1382C>G
|
ENSP00000496124.1:n.*1382C>G
|
|
|
ENST00000643925.1:c.1530C>G
|
|
|
|
ENST00000644447.1:c.1762C>G
|
ENSP00000496282.1:p.Pro588Ala
|
|
|
ENST00000644484.1:c.*1661C>G
|
ENSP00000493558.1:n.*1661C>G
|
|
|
ENST00000644675.1:c.*1578C>G
|
ENSP00000494567.1:n.*1578C>G
|
|
|
ENST00000644757.1:c.*1691C>G
|
ENSP00000495085.1:n.*1691C>G
|
|
|
ENST00000644772.1:c.3472C>G
|
ENSP00000494321.1:p.Pro1158Ala
|
|
|
ENST00000645004.1:n.545C>G
|
|
|
|
ENST00000645076.1:c.2605C>G
|
|
|
|
ENST00000645417.1:c.572C>G
|
|
|
|
ENST00000645744.1:c.*1670C>G
|
ENSP00000494564.1:n.*1670C>G
|
|
|
ENST00000645760.1:c.3681C>G
|
|
|
|
ENST00000645884.1:c.*543C>G
|
ENSP00000495516.1:n.*543C>G
|
|
|
ENST00000646003.1:c.*1362C>G
|
ENSP00000495259.1:n.*1362C>G
|
|
|
ENST00000646207.1:c.*1873C>G
|
ENSP00000495025.1:n.*1873C>G
|
|
|
ENST00000646276.1:c.*1679C>G
|
ENSP00000496070.1:n.*1679C>G
|
|
|
ENST00000646592.1:c.2712C>G
|
|
|
|
ENST00000646902.1:c.3403C>G
|
ENSP00000494101.1:p.Pro1135Ala
|
|
|
ENST00000646993.1:c.*1802C>G
|
ENSP00000493720.1:n.*1802C>G
|
|
|
ENST00000647013.1:c.3412C>G
|
ENSP00000496741.1:n.3412C>G
|
|
|
ENST00000647015.1:c.3157C>G
|
ENSP00000495389.1:p.Pro1053Ala
|
|
|
ENST00000647086.1:c.*3136C>G
|
ENSP00000493677.1:n.*3136C>G
|
|
|
ENST00000647158.1:c.*1547C>G
|
ENSP00000495744.1:n.*1547C>G
|
|
|
ENST00000302539.8:c.3409C>G
|
ENSP00000303960.4:p.Pro1137Ala
|
|
|
ENST00000389817.7:c.3406C>G
|
ENSP00000374467.3:p.Pro1136Ala
|
|
|
ENST00000524561.1:n.538C>G
|
|
|
|
ENST00000527905.5:c.*282C>G
|
ENSP00000431653.1:n.*282C>G
|
|
|
NM_000352.4:c.3406C>G
|
NP_000343.2:p.Pro1136Ala
|
|
|
NM_001287174.1:c.3409C>G
|
NP_001274103.1:p.Pro1137Ala
|
|
|
XM_011520331.1:c.3406C>G
|
XP_011518633.1:p.Pro1136Ala
|
|
|
XM_011520332.1:c.3409C>G
|
XP_011518634.1:p.Pro1137Ala
|
|
|
XM_011520333.1:c.1906C>G
|
XP_011518635.1:p.Pro636Ala
|
|
|
XR_930890.1:n.3472C>G
|
|
|
|
XR_930891.1:n.3473C>G
|
|
|
|
XR_930892.1:n.3372C>G
|
|
|
|
XR_930893.1:n.3369C>G
|
|
|
|
NM_001351295.1:c.3472C>G
|
NP_001338224.1:p.Pro1158Ala
|
|
|
NM_001351296.1:c.3406C>G
|
NP_001338225.1:p.Pro1136Ala
|
|
|
NM_001351297.1:c.3403C>G
|
NP_001338226.1:p.Pro1135Ala
|
|
|
NR_147094.1:n.3555C>G
|
|
|
|
XM_017018197.2:c.3475C>G
|
XP_016873686.1:p.Pro1159Ala
|
|
|
XM_017018199.1:c.3472C>G
|
XP_016873688.1:p.Pro1158Ala
|
|
|
XM_017018201.2:c.3475C>G
|
XP_016873690.1:p.Pro1159Ala
|
|
|
XM_017018202.1:c.1972C>G
|
XP_016873691.1:p.Pro658Ala
|
|
|
XM_017018204.1:c.1363C>G
|
XP_016873693.1:p.Pro455Ala
|
|
|
XM_024448668.1:c.1774C>G
|
XP_024304436.1:p.Pro592Ala
|
|
|
XR_001747945.2:n.3547C>G
|
|
|
|
XR_001747946.2:n.3478C>G
|
|
|
|
XR_002957189.1:n.3627C>G
|
|
|
|
NM_000352.6:c.3406C>G
MANE Select
|
NP_000343.2:p.Pro1136Ala
|
|
|
NM_001287174.2:c.3409C>G
|
NP_001274103.1:p.Pro1137Ala
|
|
|
NM_001351295.2:c.3472C>G
|
NP_001338224.1:p.Pro1158Ala
|
|
|
NM_001351296.2:c.3406C>G
|
NP_001338225.1:p.Pro1136Ala
|
|
|
NM_001351297.2:c.3403C>G
|
NP_001338226.1:p.Pro1135Ala
|
|
|
NR_147094.2:n.3555C>G
|
|
|
|
NM_001287174.3:c.3409C>G
|
NP_001274103.1:p.Pro1137Ala
|
|
