ENST00000357578.8:c.1298T>G
MANE Select
|
ENSP00000350191.3:p.Leu433Arg
|
|
ENST00000479394.2:n.413T>G
|
|
|
ENST00000672352.1:c.917T>G
|
ENSP00000500876.1:p.Leu306Arg
|
|
ENST00000672652.1:c.1261T>G
|
|
|
ENST00000348925.2:c.1337T>G
|
ENSP00000314649.3:p.Leu446Arg
|
|
ENST00000357578.7:c.1298T>G
|
ENSP00000350191.3:p.Leu433Arg
|
|
ENST00000479394.1:n.413T>G
|
|
|
ENST00000491546.5:c.1214T>G
|
ENSP00000417687.1:p.Leu405Arg
|
|
NM_001080.3:c.1298T>G
MANE Select
|
NP_001071.1:p.Leu433Arg
|
|
NM_170740.1:c.1337T>G
|
NP_733936.1:p.Leu446Arg
|
|
NM_001368954.1:c.1154T>G
|
NP_001355883.1:p.Leu385Arg
|
|