ENST00000283179.14:c.294T>G
|
ENSP00000283179.10:p.Ala98=
|
|
ENST00000444376.7:c.294T>G
|
ENSP00000393151.2:p.Ala98=
|
|
ENST00000476241.2:n.479T>G
|
|
|
ENST00000638475.1:c.78T>G
|
ENSP00000491305.1:p.Ala26=
|
|
ENST00000638952.1:n.525T>G
|
|
|
ENST00000640218.2:c.294T>G
MANE Select
|
ENSP00000491215.1:p.Ala98=
|
|
ENST00000640306.1:c.294T>G
|
ENSP00000491685.1:p.Ala98=
|
|
ENST00000649899.1:n.518T>G
|
|
|
ENST00000283179.13:c.294T>G
|
ENSP00000283179.9:p.Ala98=
|
|
ENST00000444376.6:c.294T>G
|
ENSP00000393151.2:p.Ala98=
|
|
ENST00000476241.1:n.478T>G
|
|
|
NM_004501.3:c.294T>G
|
NP_004492.2:p.Ala98=
|
|
NM_031844.2:c.294T>G
|
NP_114032.2:p.Ala98=
|
|
NM_031844.3:c.294T>G
MANE Select
|
NP_114032.2:p.Ala98=
|
|