ENST00000350026.11:c.3948A>T
|
ENSP00000055163.8:p.Ser1316=
|
|
ENST00000414678.8:c.4017A>T
|
ENSP00000412835.3:p.Ser1339=
|
|
ENST00000637015.2:c.4236A>T
|
ENSP00000489729.2:p.Ser1412=
|
|
ENST00000346085.10:c.3987A>T
|
ENSP00000344546.5:p.Ser1329=
|
|
ENST00000350026.10:c.3699A>T
|
ENSP00000055163.7:p.Ser1233=
|
|
ENST00000414678.7:c.2265A>T
|
ENSP00000412835.2:p.Ser755=
|
|
ENST00000635849.1:c.1428A>T
|
ENSP00000490948.1:p.Ser476=
|
|
ENST00000635957.1:c.1059A>T
|
ENSP00000490385.1:p.Ser353=
|
|
ENST00000636930.2:c.4107A>T
MANE Select
|
ENSP00000490491.2:p.Ser1369=
|
|
ENST00000636940.1:n.2104A>T
|
|
|
ENST00000637015.1:c.1475A>T
|
|
|
ENST00000637568.1:c.1389A>T
|
|
|
ENST00000637741.1:n.773A>T
|
|
|
ENST00000637810.1:c.1449A>T
|
ENSP00000489636.1:p.Ser483=
|
|
ENST00000637904.1:c.1608A>T
|
ENSP00000490550.1:p.Ser536=
|
|
ENST00000647938.1:c.3738A>T
|
ENSP00000498155.1:p.Ser1246=
|
|
ENST00000346085.9:c.3738A>T
|
ENSP00000344546.4:p.Ser1246=
|
|
ENST00000350026.9:c.3699A>T
|
ENSP00000055163.7:p.Ser1233=
|
|
ENST00000414678.6:c.2265A>T
|
ENSP00000412835.2:p.Ser755=
|
|
NM_017519.2:c.3699A>T
|
NP_059989.2:p.Ser1233=
|
|
NM_020732.3:c.3738A>T
|
NP_065783.3:p.Ser1246=
|
|
XM_005267069.3:c.3858A>T
|
XP_005267126.2:p.Ser1286=
|
|
XM_011535984.1:c.2937A>T
|
XP_011534286.1:p.Ser979=
|
|
XM_011535985.1:c.2757A>T
|
XP_011534287.1:p.Ser919=
|
|
XM_011535986.1:c.2517A>T
|
XP_011534288.1:p.Ser839=
|
|
XM_011535987.1:c.2136A>T
|
XP_011534289.1:p.Ser712=
|
|
XM_011535988.1:c.999A>T
|
XP_011534290.1:p.Ser333=
|
|
NM_001346813.1:c.3858A>T
|
NP_001333742.1:p.Ser1286=
|
|
NM_001363725.1:c.1608A>T
|
NP_001350654.1:p.Ser536=
|
|
XM_011535984.2:c.4068A>T
|
XP_011534286.2:p.Ser1356=
|
|
XM_011535988.3:c.999A>T
|
XP_011534290.1:p.Ser333=
|
|
XM_017011103.2:c.3969A>T
|
XP_016866592.1:p.Ser1323=
|
|
XM_017011104.1:c.3939A>T
|
XP_016866593.1:p.Ser1313=
|
|
XM_017011105.2:c.3909A>T
|
XP_016866594.1:p.Ser1303=
|
|
XM_017011106.2:c.3780A>T
|
XP_016866595.1:p.Ser1260=
|
|
XM_017011107.2:c.3759A>T
|
XP_016866596.1:p.Ser1253=
|
|
XR_002956289.1:n.4151A>T
|
|
|
NM_001363725.2:c.1608A>T
|
NP_001350654.1:p.Ser536=
|
|
NM_001371656.1:c.3987A>T
|
NP_001358585.1:p.Ser1329=
|
|
NM_001374820.1:c.3987A>T
|
NP_001361749.1:p.Ser1329=
|
|
NM_001374828.1:c.4107A>T
MANE Select
|
NP_001361757.1:p.Ser1369=
|
|
NM_017519.3:c.3948A>T
|
NP_059989.3:p.Ser1316=
|
|