ENST00000350026.11:c.3800C>A
|
ENSP00000055163.8:p.Ser1267Ter
|
|
ENST00000414678.8:c.3869C>A
|
ENSP00000412835.3:p.Ser1290Ter
|
|
ENST00000637015.2:c.4088C>A
|
ENSP00000489729.2:p.Ser1363Ter
|
|
ENST00000346085.10:c.3839C>A
|
ENSP00000344546.5:p.Ser1280Ter
|
|
ENST00000350026.10:c.3551C>A
|
ENSP00000055163.7:p.Ser1184Ter
|
|
ENST00000414678.7:c.2117C>A
|
ENSP00000412835.2:p.Ser706Ter
|
|
ENST00000635849.1:c.1280C>A
|
ENSP00000490948.1:p.Ser427Ter
|
|
ENST00000635957.1:c.914C>A
|
ENSP00000490385.1:p.Ser305Ter
|
|
ENST00000636930.2:c.3959C>A
MANE Select
|
ENSP00000490491.2:p.Ser1320Ter
|
|
ENST00000636940.1:n.1956C>A
|
|
|
ENST00000637015.1:c.1327C>A
|
|
|
ENST00000637568.1:c.1241C>A
|
|
|
ENST00000637741.1:n.625C>A
|
|
|
ENST00000637810.1:c.1301C>A
|
ENSP00000489636.1:p.Ser434Ter
|
|
ENST00000637904.1:c.1460C>A
|
ENSP00000490550.1:p.Ser487Ter
|
|
ENST00000647938.1:c.3590C>A
|
ENSP00000498155.1:p.Ser1197Ter
|
|
ENST00000346085.9:c.3590C>A
|
ENSP00000344546.4:p.Ser1197Ter
|
|
ENST00000350026.9:c.3551C>A
|
ENSP00000055163.7:p.Ser1184Ter
|
|
ENST00000414678.6:c.2117C>A
|
ENSP00000412835.2:p.Ser706Ter
|
|
NM_017519.2:c.3551C>A
|
NP_059989.2:p.Ser1184Ter
|
|
NM_020732.3:c.3590C>A
|
NP_065783.3:p.Ser1197Ter
|
|
XM_005267069.3:c.3710C>A
|
XP_005267126.2:p.Ser1237Ter
|
|
XM_011535984.1:c.2789C>A
|
XP_011534286.1:p.Ser930Ter
|
|
XM_011535985.1:c.2609C>A
|
XP_011534287.1:p.Ser870Ter
|
|
XM_011535986.1:c.2369C>A
|
XP_011534288.1:p.Ser790Ter
|
|
XM_011535987.1:c.1988C>A
|
XP_011534289.1:p.Ser663Ter
|
|
XM_011535988.1:c.851C>A
|
XP_011534290.1:p.Ser284Ter
|
|
NM_001346813.1:c.3710C>A
|
NP_001333742.1:p.Ser1237Ter
|
|
NM_001363725.1:c.1460C>A
|
NP_001350654.1:p.Ser487Ter
|
|
XM_011535984.2:c.3920C>A
|
XP_011534286.2:p.Ser1307Ter
|
|
XM_011535988.3:c.851C>A
|
XP_011534290.1:p.Ser284Ter
|
|
XM_017011103.2:c.3821C>A
|
XP_016866592.1:p.Ser1274Ter
|
|
XM_017011104.1:c.3791C>A
|
XP_016866593.1:p.Ser1264Ter
|
|
XM_017011105.2:c.3761C>A
|
XP_016866594.1:p.Ser1254Ter
|
|
XM_017011106.2:c.3632C>A
|
XP_016866595.1:p.Ser1211Ter
|
|
XM_017011107.2:c.3611C>A
|
XP_016866596.1:p.Ser1204Ter
|
|
XR_002956289.1:n.4003C>A
|
|
|
NM_001363725.2:c.1460C>A
|
NP_001350654.1:p.Ser487Ter
|
|
NM_001371656.1:c.3839C>A
|
NP_001358585.1:p.Ser1280Ter
|
|
NM_001374820.1:c.3839C>A
|
NP_001361749.1:p.Ser1280Ter
|
|
NM_001374828.1:c.3959C>A
MANE Select
|
NP_001361757.1:p.Ser1320Ter
|
|
NM_017519.3:c.3800C>A
|
NP_059989.3:p.Ser1267Ter
|
|