ENST00000328300.11:c.4032T>G
MANE Select
|
ENSP00000331902.7:p.Ser1344Arg
|
|
ENST00000361603.7:c.4014T>G
|
ENSP00000354505.2:p.Ser1338Arg
|
|
ENST00000510690.2:n.526T>G
|
|
|
ENST00000328300.10:c.4032T>G
|
ENSP00000331902.6:p.Ser1344Arg
|
|
ENST00000361603.6:c.4014T>G
|
ENSP00000354505.2:p.Ser1338Arg
|
|
ENST00000489230.1:n.435T>G
|
|
|
NM_000495.4:c.4014T>G
|
NP_000486.1:p.Ser1338Arg
|
|
NM_033380.2:c.4032T>G
|
NP_203699.1:p.Ser1344Arg
|
|
XM_005262070.2:c.4023T>G
|
XP_005262127.1:p.Ser1341Arg
|
|
XM_006724616.2:c.4032T>G
|
XP_006724679.1:p.Ser1344Arg
|
|
XM_011530849.1:c.3708T>G
|
XP_011529151.1:p.Ser1236Arg
|
|
XM_011530851.1:c.1605T>G
|
XP_011529153.1:p.Ser535Arg
|
|
XM_011530849.2:c.4047T>G
|
XP_011529151.2:p.Ser1349Arg
|
|
XM_017029259.2:c.4038T>G
|
XP_016884748.1:p.Ser1346Arg
|
|
XM_017029260.1:c.4029T>G
|
XP_016884749.1:p.Ser1343Arg
|
|
XM_017029263.2:c.2367T>G
|
XP_016884752.1:p.Ser789Arg
|
|
NM_000495.5:c.4014T>G
|
NP_000486.1:p.Ser1338Arg
|
|
NM_033380.3:c.4032T>G
MANE Select
|
NP_203699.1:p.Ser1344Arg
|
|