ENST00000280362.8:c.168G>T
MANE Select
|
ENSP00000280362.3:p.Val56=
|
|
ENST00000280362.7:c.168G>T
|
ENSP00000280362.3:p.Val56=
|
|
ENST00000524931.1:c.-37G>T
|
ENSP00000434688.1:n.-37G>T
|
|
ENST00000525803.1:c.163+1539G>T
|
ENSP00000431750.1:n.163+1539G>T
|
|
ENST00000528679.5:c.164-414G>T
|
ENSP00000435895.1:n.164-414G>T
|
|
ENST00000531175.1:n.119G>T
|
|
|
ENST00000531673.5:c.164-414G>T
|
ENSP00000433469.1:n.164-414G>T
|
|
NM_000317.2:c.168G>T
|
NP_000308.1:p.Val56=
|
|
XM_011542943.1:c.129G>T
|
XP_011541245.1:p.Val43=
|
|
NM_000317.3:c.168G>T
MANE Select
|
NP_000308.1:p.Val56=
|
|