NM_001080.3:c.1597G=
MANE Select
|
NP_001071.1:p.Gly533=
|
ENST00000357578.8:c.1597G=
MANE Select
|
ENSP00000350191.3:p.Gly533=
|
NM_001368954.1:c.1453G=
|
NP_001355883.1:p.Gly485=
|
NM_170740.1:c.1636G=
|
NP_733936.1:p.Gly546=
|
ENST00000348925.2:c.1636G=
|
ENSP00000314649.3:p.Gly546=
|
ENST00000357578.7:c.1597G=
|
ENSP00000350191.3:p.Gly533=
|
ENST00000479394.1:n.712G=
|
|
ENST00000479394.2:n.712G=
|
|
ENST00000491546.5:c.1513G=
|
ENSP00000417687.1:p.Gly505=
|
ENST00000492697.1:n.363G=
|
|
ENST00000672352.1:c.1216G=
|
ENSP00000500876.1:p.Gly406=
|
ENST00000672652.1:c.1560G=
|
|