ENST00000350026.11:c.3799T>A
|
ENSP00000055163.8:p.Ser1267Thr
|
|
ENST00000414678.8:c.3868T>A
|
ENSP00000412835.3:p.Ser1290Thr
|
|
ENST00000637015.2:c.4087T>A
|
ENSP00000489729.2:p.Ser1363Thr
|
|
ENST00000346085.10:c.3838T>A
|
ENSP00000344546.5:p.Ser1280Thr
|
|
ENST00000350026.10:c.3550T>A
|
ENSP00000055163.7:p.Ser1184Thr
|
|
ENST00000414678.7:c.2116T>A
|
ENSP00000412835.2:p.Ser706Thr
|
|
ENST00000635849.1:c.1279T>A
|
ENSP00000490948.1:p.Ser427Thr
|
|
ENST00000635957.1:c.913T>A
|
ENSP00000490385.1:p.Ser305Thr
|
|
ENST00000636930.2:c.3958T>A
MANE Select
|
ENSP00000490491.2:p.Ser1320Thr
|
|
ENST00000636940.1:n.1955T>A
|
|
|
ENST00000637015.1:c.1326T>A
|
|
|
ENST00000637568.1:c.1240T>A
|
|
|
ENST00000637741.1:n.624T>A
|
|
|
ENST00000637810.1:c.1300T>A
|
ENSP00000489636.1:p.Ser434Thr
|
|
ENST00000637904.1:c.1459T>A
|
ENSP00000490550.1:p.Ser487Thr
|
|
ENST00000647938.1:c.3589T>A
|
ENSP00000498155.1:p.Ser1197Thr
|
|
ENST00000346085.9:c.3589T>A
|
ENSP00000344546.4:p.Ser1197Thr
|
|
ENST00000350026.9:c.3550T>A
|
ENSP00000055163.7:p.Ser1184Thr
|
|
ENST00000414678.6:c.2116T>A
|
ENSP00000412835.2:p.Ser706Thr
|
|
NM_017519.2:c.3550T>A
|
NP_059989.2:p.Ser1184Thr
|
|
NM_020732.3:c.3589T>A
|
NP_065783.3:p.Ser1197Thr
|
|
XM_005267069.3:c.3709T>A
|
XP_005267126.2:p.Ser1237Thr
|
|
XM_011535984.1:c.2788T>A
|
XP_011534286.1:p.Ser930Thr
|
|
XM_011535985.1:c.2608T>A
|
XP_011534287.1:p.Ser870Thr
|
|
XM_011535986.1:c.2368T>A
|
XP_011534288.1:p.Ser790Thr
|
|
XM_011535987.1:c.1987T>A
|
XP_011534289.1:p.Ser663Thr
|
|
XM_011535988.1:c.850T>A
|
XP_011534290.1:p.Ser284Thr
|
|
NM_001346813.1:c.3709T>A
|
NP_001333742.1:p.Ser1237Thr
|
|
NM_001363725.1:c.1459T>A
|
NP_001350654.1:p.Ser487Thr
|
|
XM_011535984.2:c.3919T>A
|
XP_011534286.2:p.Ser1307Thr
|
|
XM_011535988.3:c.850T>A
|
XP_011534290.1:p.Ser284Thr
|
|
XM_017011103.2:c.3820T>A
|
XP_016866592.1:p.Ser1274Thr
|
|
XM_017011104.1:c.3790T>A
|
XP_016866593.1:p.Ser1264Thr
|
|
XM_017011105.2:c.3760T>A
|
XP_016866594.1:p.Ser1254Thr
|
|
XM_017011106.2:c.3631T>A
|
XP_016866595.1:p.Ser1211Thr
|
|
XM_017011107.2:c.3610T>A
|
XP_016866596.1:p.Ser1204Thr
|
|
XR_002956289.1:n.4002T>A
|
|
|
NM_001363725.2:c.1459T>A
|
NP_001350654.1:p.Ser487Thr
|
|
NM_001371656.1:c.3838T>A
|
NP_001358585.1:p.Ser1280Thr
|
|
NM_001374820.1:c.3838T>A
|
NP_001361749.1:p.Ser1280Thr
|
|
NM_001374828.1:c.3958T>A
MANE Select
|
NP_001361757.1:p.Ser1320Thr
|
|
NM_017519.3:c.3799T>A
|
NP_059989.3:p.Ser1267Thr
|
|