ENST00000357578.8:c.1297C>A
MANE Select
|
ENSP00000350191.3:p.Leu433Met
|
|
ENST00000479394.2:n.412C>A
|
|
|
ENST00000672352.1:c.916C>A
|
ENSP00000500876.1:p.Leu306Met
|
|
ENST00000672652.1:c.1260C>A
|
|
|
ENST00000348925.2:c.1336C>A
|
ENSP00000314649.3:p.Leu446Met
|
|
ENST00000357578.7:c.1297C>A
|
ENSP00000350191.3:p.Leu433Met
|
|
ENST00000479394.1:n.412C>A
|
|
|
ENST00000491546.5:c.1213C>A
|
ENSP00000417687.1:p.Leu405Met
|
|
NM_001080.3:c.1297C>A
MANE Select
|
NP_001071.1:p.Leu433Met
|
|
NM_170740.1:c.1336C>A
|
NP_733936.1:p.Leu446Met
|
|
NM_001368954.1:c.1153C>A
|
NP_001355883.1:p.Leu385Met
|
|