ENST00000280362.8:c.295T>G
MANE Select
|
ENSP00000280362.3:p.Tyr99Asp
|
|
ENST00000280362.7:c.295T>G
|
ENSP00000280362.3:p.Tyr99Asp
|
|
ENST00000524931.1:c.91T>G
|
ENSP00000434688.1:p.Tyr31Asp
|
|
ENST00000525803.1:c.*29T>G
|
ENSP00000431750.1:n.*29T>G
|
|
ENST00000527428.5:n.469T>G
|
|
|
ENST00000527635.1:n.336T>G
|
|
|
ENST00000528679.5:c.*104T>G
|
ENSP00000435895.1:n.*104T>G
|
|
ENST00000531175.1:n.246T>G
|
|
|
ENST00000531673.5:c.*104T>G
|
ENSP00000433469.1:n.*104T>G
|
|
NM_000317.2:c.295T>G
|
NP_000308.1:p.Tyr99Asp
|
|
XM_011542943.1:c.256T>G
|
XP_011541245.1:p.Tyr86Asp
|
|
NM_000317.3:c.295T>G
MANE Select
|
NP_000308.1:p.Tyr99Asp
|
|