ENST00000283179.14:c.262G=
|
ENSP00000283179.10:p.Glu88=
|
|
ENST00000444376.7:c.262G=
|
ENSP00000393151.2:p.Glu88=
|
|
ENST00000476241.2:n.447G=
|
|
|
ENST00000638475.1:c.46G=
|
ENSP00000491305.1:p.Glu16=
|
|
ENST00000638952.1:n.493G=
|
|
|
ENST00000640218.2:c.262G=
MANE Select
|
ENSP00000491215.1:p.Glu88=
|
|
ENST00000640306.1:c.262G=
|
ENSP00000491685.1:p.Glu88=
|
|
ENST00000649899.1:n.486G=
|
|
|
ENST00000283179.13:c.262G=
|
ENSP00000283179.9:p.Glu88=
|
|
ENST00000444376.6:c.262G=
|
ENSP00000393151.2:p.Glu88=
|
|
ENST00000476241.1:n.446G=
|
|
|
NM_004501.3:c.262G=
|
NP_004492.2:p.Glu88=
|
|
NM_031844.2:c.262G=
|
NP_114032.2:p.Glu88=
|
|
NM_031844.3:c.262G=
MANE Select
|
NP_114032.2:p.Glu88=
|
|