ENST00000704074.1:c.297C>T
|
|
|
ENST00000283179.14:c.619C>T
|
ENSP00000283179.10:p.Gln207Ter
|
|
ENST00000444376.7:c.619C>T
|
ENSP00000393151.2:p.Gln207Ter
|
|
ENST00000476241.2:n.804C>T
|
|
|
ENST00000638475.1:c.403C>T
|
ENSP00000491305.1:p.Gln135Ter
|
|
ENST00000638952.1:n.850C>T
|
|
|
ENST00000640218.2:c.619C>T
MANE Select
|
ENSP00000491215.1:p.Gln207Ter
|
|
ENST00000640306.1:c.619C>T
|
ENSP00000491685.1:p.Gln207Ter
|
|
ENST00000640440.1:c.319C>T
|
ENSP00000491263.1:p.Gln107Ter
|
|
ENST00000649899.1:n.843C>T
|
|
|
ENST00000283179.13:c.619C>T
|
ENSP00000283179.9:p.Gln207Ter
|
|
ENST00000444376.6:c.619C>T
|
ENSP00000393151.2:p.Gln207Ter
|
|
ENST00000476241.1:n.803C>T
|
|
|
NM_004501.3:c.619C>T
|
NP_004492.2:p.Gln207Ter
|
|
NM_031844.2:c.619C>T
|
NP_114032.2:p.Gln207Ter
|
|
NM_031844.3:c.619C>T
MANE Select
|
NP_114032.2:p.Gln207Ter
|
|