ENST00000350026.11:c.3969C>T
|
ENSP00000055163.8:p.Ser1323=
|
|
ENST00000414678.8:c.4038C>T
|
ENSP00000412835.3:p.Ser1346=
|
|
ENST00000637015.2:c.4257C>T
|
ENSP00000489729.2:p.Ser1419=
|
|
ENST00000346085.10:c.4008C>T
|
ENSP00000344546.5:p.Ser1336=
|
|
ENST00000350026.10:c.3720C>T
|
ENSP00000055163.7:p.Ser1240=
|
|
ENST00000414678.7:c.2286C>T
|
ENSP00000412835.2:p.Ser762=
|
|
ENST00000635849.1:c.1449C>T
|
ENSP00000490948.1:p.Ser483=
|
|
ENST00000635957.1:c.1080C>T
|
ENSP00000490385.1:p.Ser360=
|
|
ENST00000636930.2:c.4128C>T
MANE Select
|
ENSP00000490491.2:p.Ser1376=
|
|
ENST00000636940.1:n.2125C>T
|
|
|
ENST00000637015.1:c.1496C>T
|
|
|
ENST00000637568.1:c.1410C>T
|
|
|
ENST00000637741.1:n.794C>T
|
|
|
ENST00000637810.1:c.1470C>T
|
ENSP00000489636.1:p.Ser490=
|
|
ENST00000637904.1:c.1629C>T
|
ENSP00000490550.1:p.Ser543=
|
|
ENST00000647938.1:c.3759C>T
|
ENSP00000498155.1:p.Ser1253=
|
|
ENST00000346085.9:c.3759C>T
|
ENSP00000344546.4:p.Ser1253=
|
|
ENST00000350026.9:c.3720C>T
|
ENSP00000055163.7:p.Ser1240=
|
|
ENST00000414678.6:c.2286C>T
|
ENSP00000412835.2:p.Ser762=
|
|
NM_017519.2:c.3720C>T
|
NP_059989.2:p.Ser1240=
|
|
NM_020732.3:c.3759C>T
|
NP_065783.3:p.Ser1253=
|
|
XM_005267069.3:c.3879C>T
|
XP_005267126.2:p.Ser1293=
|
|
XM_011535984.1:c.2958C>T
|
XP_011534286.1:p.Ser986=
|
|
XM_011535985.1:c.2778C>T
|
XP_011534287.1:p.Ser926=
|
|
XM_011535986.1:c.2538C>T
|
XP_011534288.1:p.Ser846=
|
|
XM_011535987.1:c.2157C>T
|
XP_011534289.1:p.Ser719=
|
|
XM_011535988.1:c.1020C>T
|
XP_011534290.1:p.Ser340=
|
|
NM_001346813.1:c.3879C>T
|
NP_001333742.1:p.Ser1293=
|
|
NM_001363725.1:c.1629C>T
|
NP_001350654.1:p.Ser543=
|
|
XM_011535984.2:c.4089C>T
|
XP_011534286.2:p.Ser1363=
|
|
XM_011535988.3:c.1020C>T
|
XP_011534290.1:p.Ser340=
|
|
XM_017011103.2:c.3990C>T
|
XP_016866592.1:p.Ser1330=
|
|
XM_017011104.1:c.3960C>T
|
XP_016866593.1:p.Ser1320=
|
|
XM_017011105.2:c.3930C>T
|
XP_016866594.1:p.Ser1310=
|
|
XM_017011106.2:c.3801C>T
|
XP_016866595.1:p.Ser1267=
|
|
XM_017011107.2:c.3780C>T
|
XP_016866596.1:p.Ser1260=
|
|
XR_002956289.1:n.4172C>T
|
|
|
NM_001363725.2:c.1629C>T
|
NP_001350654.1:p.Ser543=
|
|
NM_001371656.1:c.4008C>T
|
NP_001358585.1:p.Ser1336=
|
|
NM_001374820.1:c.4008C>T
|
NP_001361749.1:p.Ser1336=
|
|
NM_001374828.1:c.4128C>T
MANE Select
|
NP_001361757.1:p.Ser1376=
|
|
NM_017519.3:c.3969C>T
|
NP_059989.3:p.Ser1323=
|
|