ENST00000350026.11:c.3902G>C
|
ENSP00000055163.8:p.Ser1301Thr
|
|
ENST00000414678.8:c.3971G>C
|
ENSP00000412835.3:p.Ser1324Thr
|
|
ENST00000637015.2:c.4190G>C
|
ENSP00000489729.2:p.Ser1397Thr
|
|
ENST00000346085.10:c.3941G>C
|
ENSP00000344546.5:p.Ser1314Thr
|
|
ENST00000350026.10:c.3653G>C
|
ENSP00000055163.7:p.Ser1218Thr
|
|
ENST00000414678.7:c.2219G>C
|
ENSP00000412835.2:p.Ser740Thr
|
|
ENST00000635849.1:c.1382G>C
|
ENSP00000490948.1:p.Ser461Thr
|
|
ENST00000635957.1:c.1014-1G>C
|
ENSP00000490385.1:n.1014-1G>C
|
|
ENST00000636930.2:c.4061G>C
MANE Select
|
ENSP00000490491.2:p.Ser1354Thr
|
|
ENST00000636940.1:n.2058G>C
|
|
|
ENST00000637015.1:c.1429G>C
|
|
|
ENST00000637568.1:c.1343G>C
|
|
|
ENST00000637741.1:n.727G>C
|
|
|
ENST00000637810.1:c.1403G>C
|
ENSP00000489636.1:p.Ser468Thr
|
|
ENST00000637904.1:c.1562G>C
|
ENSP00000490550.1:p.Ser521Thr
|
|
ENST00000647938.1:c.3692G>C
|
ENSP00000498155.1:p.Ser1231Thr
|
|
ENST00000346085.9:c.3692G>C
|
ENSP00000344546.4:p.Ser1231Thr
|
|
ENST00000350026.9:c.3653G>C
|
ENSP00000055163.7:p.Ser1218Thr
|
|
ENST00000414678.6:c.2219G>C
|
ENSP00000412835.2:p.Ser740Thr
|
|
NM_017519.2:c.3653G>C
|
NP_059989.2:p.Ser1218Thr
|
|
NM_020732.3:c.3692G>C
|
NP_065783.3:p.Ser1231Thr
|
|
XM_005267069.3:c.3812G>C
|
XP_005267126.2:p.Ser1271Thr
|
|
XM_011535984.1:c.2891G>C
|
XP_011534286.1:p.Ser964Thr
|
|
XM_011535985.1:c.2711G>C
|
XP_011534287.1:p.Ser904Thr
|
|
XM_011535986.1:c.2471G>C
|
XP_011534288.1:p.Ser824Thr
|
|
XM_011535987.1:c.2090G>C
|
XP_011534289.1:p.Ser697Thr
|
|
XM_011535988.1:c.953G>C
|
XP_011534290.1:p.Ser318Thr
|
|
NM_001346813.1:c.3812G>C
|
NP_001333742.1:p.Ser1271Thr
|
|
NM_001363725.1:c.1562G>C
|
NP_001350654.1:p.Ser521Thr
|
|
XM_011535984.2:c.4022G>C
|
XP_011534286.2:p.Ser1341Thr
|
|
XM_011535988.3:c.953G>C
|
XP_011534290.1:p.Ser318Thr
|
|
XM_017011103.2:c.3923G>C
|
XP_016866592.1:p.Ser1308Thr
|
|
XM_017011104.1:c.3893G>C
|
XP_016866593.1:p.Ser1298Thr
|
|
XM_017011105.2:c.3863G>C
|
XP_016866594.1:p.Ser1288Thr
|
|
XM_017011106.2:c.3734G>C
|
XP_016866595.1:p.Ser1245Thr
|
|
XM_017011107.2:c.3713G>C
|
XP_016866596.1:p.Ser1238Thr
|
|
XR_002956289.1:n.4105G>C
|
|
|
NM_001363725.2:c.1562G>C
|
NP_001350654.1:p.Ser521Thr
|
|
NM_001371656.1:c.3941G>C
|
NP_001358585.1:p.Ser1314Thr
|
|
NM_001374820.1:c.3941G>C
|
NP_001361749.1:p.Ser1314Thr
|
|
NM_001374828.1:c.4061G>C
MANE Select
|
NP_001361757.1:p.Ser1354Thr
|
|
NM_017519.3:c.3902G>C
|
NP_059989.3:p.Ser1301Thr
|
|