ENST00000350026.11:c.3808A>T
|
ENSP00000055163.8:p.Ser1270Cys
|
|
ENST00000414678.8:c.3877A>T
|
ENSP00000412835.3:p.Ser1293Cys
|
|
ENST00000637015.2:c.4096A>T
|
ENSP00000489729.2:p.Ser1366Cys
|
|
ENST00000346085.10:c.3847A>T
|
ENSP00000344546.5:p.Ser1283Cys
|
|
ENST00000350026.10:c.3559A>T
|
ENSP00000055163.7:p.Ser1187Cys
|
|
ENST00000414678.7:c.2125A>T
|
ENSP00000412835.2:p.Ser709Cys
|
|
ENST00000635849.1:c.1288A>T
|
ENSP00000490948.1:p.Ser430Cys
|
|
ENST00000635957.1:c.922A>T
|
ENSP00000490385.1:p.Ser308Cys
|
|
ENST00000636930.2:c.3967A>T
MANE Select
|
ENSP00000490491.2:p.Ser1323Cys
|
|
ENST00000636940.1:n.1964A>T
|
|
|
ENST00000637015.1:c.1335A>T
|
|
|
ENST00000637568.1:c.1249A>T
|
|
|
ENST00000637741.1:n.633A>T
|
|
|
ENST00000637810.1:c.1309A>T
|
ENSP00000489636.1:p.Ser437Cys
|
|
ENST00000637904.1:c.1468A>T
|
ENSP00000490550.1:p.Ser490Cys
|
|
ENST00000647938.1:c.3598A>T
|
ENSP00000498155.1:p.Ser1200Cys
|
|
ENST00000346085.9:c.3598A>T
|
ENSP00000344546.4:p.Ser1200Cys
|
|
ENST00000350026.9:c.3559A>T
|
ENSP00000055163.7:p.Ser1187Cys
|
|
ENST00000414678.6:c.2125A>T
|
ENSP00000412835.2:p.Ser709Cys
|
|
NM_017519.2:c.3559A>T
|
NP_059989.2:p.Ser1187Cys
|
|
NM_020732.3:c.3598A>T
|
NP_065783.3:p.Ser1200Cys
|
|
XM_005267069.3:c.3718A>T
|
XP_005267126.2:p.Ser1240Cys
|
|
XM_011535984.1:c.2797A>T
|
XP_011534286.1:p.Ser933Cys
|
|
XM_011535985.1:c.2617A>T
|
XP_011534287.1:p.Ser873Cys
|
|
XM_011535986.1:c.2377A>T
|
XP_011534288.1:p.Ser793Cys
|
|
XM_011535987.1:c.1996A>T
|
XP_011534289.1:p.Ser666Cys
|
|
XM_011535988.1:c.859A>T
|
XP_011534290.1:p.Ser287Cys
|
|
NM_001346813.1:c.3718A>T
|
NP_001333742.1:p.Ser1240Cys
|
|
NM_001363725.1:c.1468A>T
|
NP_001350654.1:p.Ser490Cys
|
|
XM_011535984.2:c.3928A>T
|
XP_011534286.2:p.Ser1310Cys
|
|
XM_011535988.3:c.859A>T
|
XP_011534290.1:p.Ser287Cys
|
|
XM_017011103.2:c.3829A>T
|
XP_016866592.1:p.Ser1277Cys
|
|
XM_017011104.1:c.3799A>T
|
XP_016866593.1:p.Ser1267Cys
|
|
XM_017011105.2:c.3769A>T
|
XP_016866594.1:p.Ser1257Cys
|
|
XM_017011106.2:c.3640A>T
|
XP_016866595.1:p.Ser1214Cys
|
|
XM_017011107.2:c.3619A>T
|
XP_016866596.1:p.Ser1207Cys
|
|
XR_002956289.1:n.4011A>T
|
|
|
NM_001363725.2:c.1468A>T
|
NP_001350654.1:p.Ser490Cys
|
|
NM_001371656.1:c.3847A>T
|
NP_001358585.1:p.Ser1283Cys
|
|
NM_001374820.1:c.3847A>T
|
NP_001361749.1:p.Ser1283Cys
|
|
NM_001374828.1:c.3967A>T
MANE Select
|
NP_001361757.1:p.Ser1323Cys
|
|
NM_017519.3:c.3808A>T
|
NP_059989.3:p.Ser1270Cys
|
|