ENST00000350026.11:c.3905G>C
|
ENSP00000055163.8:p.Ser1302Thr
|
|
ENST00000414678.8:c.3974G>C
|
ENSP00000412835.3:p.Ser1325Thr
|
|
ENST00000637015.2:c.4193G>C
|
ENSP00000489729.2:p.Ser1398Thr
|
|
ENST00000346085.10:c.3944G>C
|
ENSP00000344546.5:p.Ser1315Thr
|
|
ENST00000350026.10:c.3656G>C
|
ENSP00000055163.7:p.Ser1219Thr
|
|
ENST00000414678.7:c.2222G>C
|
ENSP00000412835.2:p.Ser741Thr
|
|
ENST00000635849.1:c.1385G>C
|
ENSP00000490948.1:p.Ser462Thr
|
|
ENST00000635957.1:c.1016G>C
|
ENSP00000490385.1:p.Ser339Thr
|
|
ENST00000636930.2:c.4064G>C
MANE Select
|
ENSP00000490491.2:p.Ser1355Thr
|
|
ENST00000636940.1:n.2061G>C
|
|
|
ENST00000637015.1:c.1432G>C
|
|
|
ENST00000637568.1:c.1346G>C
|
|
|
ENST00000637741.1:n.730G>C
|
|
|
ENST00000637810.1:c.1406G>C
|
ENSP00000489636.1:p.Ser469Thr
|
|
ENST00000637904.1:c.1565G>C
|
ENSP00000490550.1:p.Ser522Thr
|
|
ENST00000647938.1:c.3695G>C
|
ENSP00000498155.1:p.Ser1232Thr
|
|
ENST00000346085.9:c.3695G>C
|
ENSP00000344546.4:p.Ser1232Thr
|
|
ENST00000350026.9:c.3656G>C
|
ENSP00000055163.7:p.Ser1219Thr
|
|
ENST00000414678.6:c.2222G>C
|
ENSP00000412835.2:p.Ser741Thr
|
|
NM_017519.2:c.3656G>C
|
NP_059989.2:p.Ser1219Thr
|
|
NM_020732.3:c.3695G>C
|
NP_065783.3:p.Ser1232Thr
|
|
XM_005267069.3:c.3815G>C
|
XP_005267126.2:p.Ser1272Thr
|
|
XM_011535984.1:c.2894G>C
|
XP_011534286.1:p.Ser965Thr
|
|
XM_011535985.1:c.2714G>C
|
XP_011534287.1:p.Ser905Thr
|
|
XM_011535986.1:c.2474G>C
|
XP_011534288.1:p.Ser825Thr
|
|
XM_011535987.1:c.2093G>C
|
XP_011534289.1:p.Ser698Thr
|
|
XM_011535988.1:c.956G>C
|
XP_011534290.1:p.Ser319Thr
|
|
NM_001346813.1:c.3815G>C
|
NP_001333742.1:p.Ser1272Thr
|
|
NM_001363725.1:c.1565G>C
|
NP_001350654.1:p.Ser522Thr
|
|
XM_011535984.2:c.4025G>C
|
XP_011534286.2:p.Ser1342Thr
|
|
XM_011535988.3:c.956G>C
|
XP_011534290.1:p.Ser319Thr
|
|
XM_017011103.2:c.3926G>C
|
XP_016866592.1:p.Ser1309Thr
|
|
XM_017011104.1:c.3896G>C
|
XP_016866593.1:p.Ser1299Thr
|
|
XM_017011105.2:c.3866G>C
|
XP_016866594.1:p.Ser1289Thr
|
|
XM_017011106.2:c.3737G>C
|
XP_016866595.1:p.Ser1246Thr
|
|
XM_017011107.2:c.3716G>C
|
XP_016866596.1:p.Ser1239Thr
|
|
XR_002956289.1:n.4108G>C
|
|
|
NM_001363725.2:c.1565G>C
|
NP_001350654.1:p.Ser522Thr
|
|
NM_001371656.1:c.3944G>C
|
NP_001358585.1:p.Ser1315Thr
|
|
NM_001374820.1:c.3944G>C
|
NP_001361749.1:p.Ser1315Thr
|
|
NM_001374828.1:c.4064G>C
MANE Select
|
NP_001361757.1:p.Ser1355Thr
|
|
NM_017519.3:c.3905G>C
|
NP_059989.3:p.Ser1302Thr
|
|