ENST00000704074.1:c.59C>T
|
|
|
ENST00000283179.14:c.381C>T
|
ENSP00000283179.10:p.Ala127=
|
|
ENST00000444376.7:c.381C>T
|
ENSP00000393151.2:p.Ala127=
|
|
ENST00000476241.2:n.566C>T
|
|
|
ENST00000638475.1:c.165C>T
|
ENSP00000491305.1:p.Ala55=
|
|
ENST00000638952.1:n.612C>T
|
|
|
ENST00000640218.2:c.381C>T
MANE Select
|
ENSP00000491215.1:p.Ala127=
|
|
ENST00000640306.1:c.381C>T
|
ENSP00000491685.1:p.Ala127=
|
|
ENST00000640440.1:c.81C>T
|
ENSP00000491263.1:p.Ala27=
|
|
ENST00000649899.1:n.605C>T
|
|
|
ENST00000283179.13:c.381C>T
|
ENSP00000283179.9:p.Ala127=
|
|
ENST00000444376.6:c.381C>T
|
ENSP00000393151.2:p.Ala127=
|
|
ENST00000476241.1:n.565C>T
|
|
|
NM_004501.3:c.381C>T
|
NP_004492.2:p.Ala127=
|
|
NM_031844.2:c.381C>T
|
NP_114032.2:p.Ala127=
|
|
NM_031844.3:c.381C>T
MANE Select
|
NP_114032.2:p.Ala127=
|
|