ENST00000350026.11:c.3968C>A
|
ENSP00000055163.8:p.Ser1323Tyr
|
|
ENST00000414678.8:c.4037C>A
|
ENSP00000412835.3:p.Ser1346Tyr
|
|
ENST00000637015.2:c.4256C>A
|
ENSP00000489729.2:p.Ser1419Tyr
|
|
ENST00000346085.10:c.4007C>A
|
ENSP00000344546.5:p.Ser1336Tyr
|
|
ENST00000350026.10:c.3719C>A
|
ENSP00000055163.7:p.Ser1240Tyr
|
|
ENST00000414678.7:c.2285C>A
|
ENSP00000412835.2:p.Ser762Tyr
|
|
ENST00000635849.1:c.1448C>A
|
ENSP00000490948.1:p.Ser483Tyr
|
|
ENST00000635957.1:c.1079C>A
|
ENSP00000490385.1:p.Ser360Tyr
|
|
ENST00000636930.2:c.4127C>A
MANE Select
|
ENSP00000490491.2:p.Ser1376Tyr
|
|
ENST00000636940.1:n.2124C>A
|
|
|
ENST00000637015.1:c.1495C>A
|
|
|
ENST00000637568.1:c.1409C>A
|
|
|
ENST00000637741.1:n.793C>A
|
|
|
ENST00000637810.1:c.1469C>A
|
ENSP00000489636.1:p.Ser490Tyr
|
|
ENST00000637904.1:c.1628C>A
|
ENSP00000490550.1:p.Ser543Tyr
|
|
ENST00000647938.1:c.3758C>A
|
ENSP00000498155.1:p.Ser1253Tyr
|
|
ENST00000346085.9:c.3758C>A
|
ENSP00000344546.4:p.Ser1253Tyr
|
|
ENST00000350026.9:c.3719C>A
|
ENSP00000055163.7:p.Ser1240Tyr
|
|
ENST00000414678.6:c.2285C>A
|
ENSP00000412835.2:p.Ser762Tyr
|
|
NM_017519.2:c.3719C>A
|
NP_059989.2:p.Ser1240Tyr
|
|
NM_020732.3:c.3758C>A
|
NP_065783.3:p.Ser1253Tyr
|
|
XM_005267069.3:c.3878C>A
|
XP_005267126.2:p.Ser1293Tyr
|
|
XM_011535984.1:c.2957C>A
|
XP_011534286.1:p.Ser986Tyr
|
|
XM_011535985.1:c.2777C>A
|
XP_011534287.1:p.Ser926Tyr
|
|
XM_011535986.1:c.2537C>A
|
XP_011534288.1:p.Ser846Tyr
|
|
XM_011535987.1:c.2156C>A
|
XP_011534289.1:p.Ser719Tyr
|
|
XM_011535988.1:c.1019C>A
|
XP_011534290.1:p.Ser340Tyr
|
|
NM_001346813.1:c.3878C>A
|
NP_001333742.1:p.Ser1293Tyr
|
|
NM_001363725.1:c.1628C>A
|
NP_001350654.1:p.Ser543Tyr
|
|
XM_011535984.2:c.4088C>A
|
XP_011534286.2:p.Ser1363Tyr
|
|
XM_011535988.3:c.1019C>A
|
XP_011534290.1:p.Ser340Tyr
|
|
XM_017011103.2:c.3989C>A
|
XP_016866592.1:p.Ser1330Tyr
|
|
XM_017011104.1:c.3959C>A
|
XP_016866593.1:p.Ser1320Tyr
|
|
XM_017011105.2:c.3929C>A
|
XP_016866594.1:p.Ser1310Tyr
|
|
XM_017011106.2:c.3800C>A
|
XP_016866595.1:p.Ser1267Tyr
|
|
XM_017011107.2:c.3779C>A
|
XP_016866596.1:p.Ser1260Tyr
|
|
XR_002956289.1:n.4171C>A
|
|
|
NM_001363725.2:c.1628C>A
|
NP_001350654.1:p.Ser543Tyr
|
|
NM_001371656.1:c.4007C>A
|
NP_001358585.1:p.Ser1336Tyr
|
|
NM_001374820.1:c.4007C>A
|
NP_001361749.1:p.Ser1336Tyr
|
|
NM_001374828.1:c.4127C>A
MANE Select
|
NP_001361757.1:p.Ser1376Tyr
|
|
NM_017519.3:c.3968C>A
|
NP_059989.3:p.Ser1323Tyr
|
|