ENST00000283179.14:c.267G>A
|
ENSP00000283179.10:p.Glu89=
|
|
ENST00000444376.7:c.267G>A
|
ENSP00000393151.2:p.Glu89=
|
|
ENST00000476241.2:n.452G>A
|
|
|
ENST00000638475.1:c.51G>A
|
ENSP00000491305.1:p.Glu17=
|
|
ENST00000638952.1:n.498G>A
|
|
|
ENST00000640218.2:c.267G>A
MANE Select
|
ENSP00000491215.1:p.Glu89=
|
|
ENST00000640306.1:c.267G>A
|
ENSP00000491685.1:p.Glu89=
|
|
ENST00000649899.1:n.491G>A
|
|
|
ENST00000283179.13:c.267G>A
|
ENSP00000283179.9:p.Glu89=
|
|
ENST00000444376.6:c.267G>A
|
ENSP00000393151.2:p.Glu89=
|
|
ENST00000476241.1:n.451G>A
|
|
|
NM_004501.3:c.267G>A
|
NP_004492.2:p.Glu89=
|
|
NM_031844.2:c.267G>A
|
NP_114032.2:p.Glu89=
|
|
NM_031844.3:c.267G>A
MANE Select
|
NP_114032.2:p.Glu89=
|
|