ENST00000283179.14:c.293C>T
|
ENSP00000283179.10:p.Ala98Val
|
|
ENST00000444376.7:c.293C>T
|
ENSP00000393151.2:p.Ala98Val
|
|
ENST00000476241.2:n.478C>T
|
|
|
ENST00000638475.1:c.77C>T
|
ENSP00000491305.1:p.Ala26Val
|
|
ENST00000638952.1:n.524C>T
|
|
|
ENST00000640218.2:c.293C>T
MANE Select
|
ENSP00000491215.1:p.Ala98Val
|
|
ENST00000640306.1:c.293C>T
|
ENSP00000491685.1:p.Ala98Val
|
|
ENST00000649899.1:n.517C>T
|
|
|
ENST00000283179.13:c.293C>T
|
ENSP00000283179.9:p.Ala98Val
|
|
ENST00000444376.6:c.293C>T
|
ENSP00000393151.2:p.Ala98Val
|
|
ENST00000476241.1:n.477C>T
|
|
|
NM_004501.3:c.293C>T
|
NP_004492.2:p.Ala98Val
|
|
NM_031844.2:c.293C>T
|
NP_114032.2:p.Ala98Val
|
|
NM_031844.3:c.293C>T
MANE Select
|
NP_114032.2:p.Ala98Val
|
|