ENST00000269980.7:c.307C>G
MANE Select
|
ENSP00000269980.2:p.Leu103Val
|
|
ENST00000269980.6:c.307C>G
|
ENSP00000269980.2:p.Leu103Val
|
|
ENST00000457836.6:c.241C>G
|
ENSP00000416000.2:p.Leu81Val
|
|
ENST00000538423.5:n.433C>G
|
|
|
ENST00000540732.3:c.409C>G
|
ENSP00000443246.1:p.Leu137Val
|
|
ENST00000541315.1:c.114C>G
|
|
|
ENST00000542943.5:c.288+125C>G
|
ENSP00000440345.1:n.288+125C>G
|
|
ENST00000595085.5:c.307C>G
|
ENSP00000471150.2:p.Leu103Val
|
|
NM_000709.3:c.307C>G
|
NP_000700.1:p.Leu103Val
|
|
NM_001164783.1:c.307C>G
|
NP_001158255.1:p.Leu103Val
|
|
NM_000709.4:c.307C>G
MANE Select
|
NP_000700.1:p.Leu103Val
|
|
NM_001164783.2:c.307C>G
|
NP_001158255.1:p.Leu103Val
|
|