ENST00000357578.8:c.1597G>C
MANE Select
|
ENSP00000350191.3:p.Gly533Arg
|
|
ENST00000479394.2:n.712G>C
|
|
|
ENST00000672352.1:c.1216G>C
|
ENSP00000500876.1:p.Gly406Arg
|
|
ENST00000672652.1:c.1560G>C
|
|
|
ENST00000348925.2:c.1636G>C
|
ENSP00000314649.3:p.Gly546Arg
|
|
ENST00000357578.7:c.1597G>C
|
ENSP00000350191.3:p.Gly533Arg
|
|
ENST00000479394.1:n.712G>C
|
|
|
ENST00000491546.5:c.1513G>C
|
ENSP00000417687.1:p.Gly505Arg
|
|
ENST00000492697.1:n.363G>C
|
|
|
NM_001080.3:c.1597G>C
MANE Select
|
NP_001071.1:p.Gly533Arg
|
|
NM_170740.1:c.1636G>C
|
NP_733936.1:p.Gly546Arg
|
|
NM_001368954.1:c.1453G>C
|
NP_001355883.1:p.Gly485Arg
|
|