ENST00000280362.8:c.347A=
MANE Select
|
ENSP00000280362.3:p.Asp116=
|
|
ENST00000280362.7:c.347A=
|
ENSP00000280362.3:p.Asp116=
|
|
ENST00000524931.1:c.143A=
|
ENSP00000434688.1:p.Asp48=
|
|
ENST00000525803.1:c.*81A=
|
ENSP00000431750.1:n.*81A=
|
|
ENST00000527428.5:n.488+231A=
|
|
|
ENST00000527635.1:n.388A=
|
|
|
ENST00000528679.5:c.*156A=
|
ENSP00000435895.1:n.*156A=
|
|
ENST00000531673.5:c.*123+231A=
|
ENSP00000433469.1:n.*123+231A=
|
|
NM_000317.2:c.347A=
|
NP_000308.1:p.Asp116=
|
|
XM_011542943.1:c.308A=
|
XP_011541245.1:p.Asp103=
|
|
NM_000317.3:c.347A=
MANE Select
|
NP_000308.1:p.Asp116=
|
|