ENST00000344265.8:c.536T>A
|
ENSP00000342931.3:p.Val179Asp
|
|
ENST00000350375.7:c.458T>A
MANE Select
|
ENSP00000263781.2:p.Val153Asp
|
|
ENST00000344265.7:c.536T>A
|
ENSP00000342931.3:p.Val179Asp
|
|
ENST00000350375.6:c.458T>A
|
ENSP00000263781.2:p.Val153Asp
|
|
ENST00000560656.1:c.439+2071T>A
|
ENSP00000452610.1:n.439+2071T>A
|
|
ENST00000561167.5:c.233T>A
|
ENSP00000454072.1:p.Val78Asp
|
|
NM_000306.3:c.458T>A
|
NP_000297.1:p.Val153Asp
|
|
NM_001122757.2:c.536T>A
|
NP_001116229.1:p.Val179Asp
|
|
NM_000306.4:c.458T>A
MANE Select
|
NP_000297.1:p.Val153Asp
|
|
NM_001122757.3:c.536T>A
|
NP_001116229.1:p.Val179Asp
|
|