ENST00000252288.8:c.429C>T
MANE Select
|
ENSP00000252288.1:p.Thr143=
|
|
ENST00000447102.8:c.429C>T
|
ENSP00000403536.2:p.Thr143=
|
|
ENST00000591788.3:c.112C>T
|
|
|
ENST00000640164.1:n.262C>T
|
|
|
ENST00000640762.1:c.360C>T
|
ENSP00000492031.1:p.Thr120=
|
|
ENST00000252288.6:c.429C>T
|
ENSP00000252288.1:p.Thr143=
|
|
ENST00000447102.7:c.429C>T
|
ENSP00000403536.2:p.Thr143=
|
|
ENST00000591788.2:c.114C>T
|
ENSP00000466341.2:p.Thr38=
|
|
NM_000156.5:c.429C>T
|
NP_000147.1:p.Thr143=
|
|
NM_138924.2:c.429C>T
|
NP_620279.1:p.Thr143=
|
|
NM_000156.6:c.429C>T
MANE Select
|
NP_000147.1:p.Thr143=
|
|
NM_138924.3:c.429C>T
|
NP_620279.1:p.Thr143=
|
|