ENST00000357578.8:c.1302C>G
MANE Select
|
ENSP00000350191.3:p.Cys434Trp
|
|
ENST00000479394.2:n.417C>G
|
|
|
ENST00000672352.1:c.921C>G
|
ENSP00000500876.1:p.Cys307Trp
|
|
ENST00000672652.1:c.1265C>G
|
|
|
ENST00000348925.2:c.1341C>G
|
ENSP00000314649.3:p.Cys447Trp
|
|
ENST00000357578.7:c.1302C>G
|
ENSP00000350191.3:p.Cys434Trp
|
|
ENST00000479394.1:n.417C>G
|
|
|
ENST00000491546.5:c.1218C>G
|
ENSP00000417687.1:p.Cys406Trp
|
|
NM_001080.3:c.1302C>G
MANE Select
|
NP_001071.1:p.Cys434Trp
|
|
NM_170740.1:c.1341C>G
|
NP_733936.1:p.Cys447Trp
|
|
NM_001368954.1:c.1158C>G
|
NP_001355883.1:p.Cys386Trp
|
|