ENST00000301761.7:c.481C>G
MANE Select
|
ENSP00000301761.3:p.Leu161Val
|
|
ENST00000301761.6:c.481C>G
|
ENSP00000301761.2:p.Leu161Val
|
|
ENST00000536670.5:n.396+7938C>G
|
|
|
ENST00000537782.5:c.*127C>G
|
ENSP00000469951.1:n.*127C>G
|
|
ENST00000538594.5:c.370+7938C>G
|
ENSP00000440939.1:n.370+7938C>G
|
|
ENST00000541135.5:c.377+7931C>G
|
ENSP00000443130.1:n.377+7931C>G
|
|
ENST00000542074.1:c.*60C>G
|
ENSP00000469670.1:n.*60C>G
|
|
ENST00000542794.5:c.*483C>G
|
ENSP00000439983.1:n.*483C>G
|
|
ENST00000543044.2:c.445C>G
|
ENSP00000440219.1:p.Leu149Val
|
|
ENST00000543265.1:c.*104C>G
|
ENSP00000443660.1:n.*104C>G
|
|
ENST00000544025.5:n.465+7938C>G
|
|
|
ENST00000544801.5:c.370+7938C>G
|
ENSP00000442581.1:n.370+7938C>G
|
|
ENST00000544880.1:n.374+7938C>G
|
|
|
NM_017841.2:c.481C>G , LRG_519t1:c.481C>G
|
NP_060311.1:p.Leu161Val
|
|
NM_017841.4:c.481C>G
MANE Select
|
NP_060311.1:p.Leu161Val
|
|