ENST00000350026.11:c.3810C>G
|
ENSP00000055163.8:p.Ser1270Arg
|
|
ENST00000414678.8:c.3879C>G
|
ENSP00000412835.3:p.Ser1293Arg
|
|
ENST00000637015.2:c.4098C>G
|
ENSP00000489729.2:p.Ser1366Arg
|
|
ENST00000346085.10:c.3849C>G
|
ENSP00000344546.5:p.Ser1283Arg
|
|
ENST00000350026.10:c.3561C>G
|
ENSP00000055163.7:p.Ser1187Arg
|
|
ENST00000414678.7:c.2127C>G
|
ENSP00000412835.2:p.Ser709Arg
|
|
ENST00000635849.1:c.1290C>G
|
ENSP00000490948.1:p.Ser430Arg
|
|
ENST00000635957.1:c.924C>G
|
ENSP00000490385.1:p.Ser308Arg
|
|
ENST00000636930.2:c.3969C>G
MANE Select
|
ENSP00000490491.2:p.Ser1323Arg
|
|
ENST00000636940.1:n.1966C>G
|
|
|
ENST00000637015.1:c.1337C>G
|
|
|
ENST00000637568.1:c.1251C>G
|
|
|
ENST00000637741.1:n.635C>G
|
|
|
ENST00000637810.1:c.1311C>G
|
ENSP00000489636.1:p.Ser437Arg
|
|
ENST00000637904.1:c.1470C>G
|
ENSP00000490550.1:p.Ser490Arg
|
|
ENST00000647938.1:c.3600C>G
|
ENSP00000498155.1:p.Ser1200Arg
|
|
ENST00000346085.9:c.3600C>G
|
ENSP00000344546.4:p.Ser1200Arg
|
|
ENST00000350026.9:c.3561C>G
|
ENSP00000055163.7:p.Ser1187Arg
|
|
ENST00000414678.6:c.2127C>G
|
ENSP00000412835.2:p.Ser709Arg
|
|
NM_017519.2:c.3561C>G
|
NP_059989.2:p.Ser1187Arg
|
|
NM_020732.3:c.3600C>G
|
NP_065783.3:p.Ser1200Arg
|
|
XM_005267069.3:c.3720C>G
|
XP_005267126.2:p.Ser1240Arg
|
|
XM_011535984.1:c.2799C>G
|
XP_011534286.1:p.Ser933Arg
|
|
XM_011535985.1:c.2619C>G
|
XP_011534287.1:p.Ser873Arg
|
|
XM_011535986.1:c.2379C>G
|
XP_011534288.1:p.Ser793Arg
|
|
XM_011535987.1:c.1998C>G
|
XP_011534289.1:p.Ser666Arg
|
|
XM_011535988.1:c.861C>G
|
XP_011534290.1:p.Ser287Arg
|
|
NM_001346813.1:c.3720C>G
|
NP_001333742.1:p.Ser1240Arg
|
|
NM_001363725.1:c.1470C>G
|
NP_001350654.1:p.Ser490Arg
|
|
XM_011535984.2:c.3930C>G
|
XP_011534286.2:p.Ser1310Arg
|
|
XM_011535988.3:c.861C>G
|
XP_011534290.1:p.Ser287Arg
|
|
XM_017011103.2:c.3831C>G
|
XP_016866592.1:p.Ser1277Arg
|
|
XM_017011104.1:c.3801C>G
|
XP_016866593.1:p.Ser1267Arg
|
|
XM_017011105.2:c.3771C>G
|
XP_016866594.1:p.Ser1257Arg
|
|
XM_017011106.2:c.3642C>G
|
XP_016866595.1:p.Ser1214Arg
|
|
XM_017011107.2:c.3621C>G
|
XP_016866596.1:p.Ser1207Arg
|
|
XR_002956289.1:n.4013C>G
|
|
|
NM_001363725.2:c.1470C>G
|
NP_001350654.1:p.Ser490Arg
|
|
NM_001371656.1:c.3849C>G
|
NP_001358585.1:p.Ser1283Arg
|
|
NM_001374820.1:c.3849C>G
|
NP_001361749.1:p.Ser1283Arg
|
|
NM_001374828.1:c.3969C>G
MANE Select
|
NP_001361757.1:p.Ser1323Arg
|
|
NM_017519.3:c.3810C>G
|
NP_059989.3:p.Ser1270Arg
|
|