ENST00000344265.8:c.848T>G
|
ENSP00000342931.3:p.Val283Gly
|
|
ENST00000350375.7:c.770T>G
MANE Select
|
ENSP00000263781.2:p.Val257Gly
|
|
ENST00000344265.7:c.848T>G
|
ENSP00000342931.3:p.Val283Gly
|
|
ENST00000350375.6:c.770T>G
|
ENSP00000263781.2:p.Val257Gly
|
|
ENST00000560656.1:c.544T>G
|
ENSP00000452610.1:n.544T>G
|
|
ENST00000561167.5:c.545T>G
|
ENSP00000454072.1:p.Val182Gly
|
|
NM_000306.3:c.770T>G
|
NP_000297.1:p.Val257Gly
|
|
NM_001122757.2:c.848T>G
|
NP_001116229.1:p.Val283Gly
|
|
NM_000306.4:c.770T>G
MANE Select
|
NP_000297.1:p.Val257Gly
|
|
NM_001122757.3:c.848T>G
|
NP_001116229.1:p.Val283Gly
|
|