ENST00000704074.1:c.211G=
|
|
|
ENST00000283179.14:c.533G=
|
ENSP00000283179.10:p.Gly178=
|
|
ENST00000444376.7:c.533G=
|
ENSP00000393151.2:p.Gly178=
|
|
ENST00000476241.2:n.718G=
|
|
|
ENST00000638475.1:c.317G=
|
ENSP00000491305.1:p.Gly106=
|
|
ENST00000638952.1:n.764G=
|
|
|
ENST00000640218.2:c.533G=
MANE Select
|
ENSP00000491215.1:p.Gly178=
|
|
ENST00000640306.1:c.533G=
|
ENSP00000491685.1:p.Gly178=
|
|
ENST00000640440.1:c.233G=
|
ENSP00000491263.1:p.Gly78=
|
|
ENST00000649899.1:n.757G=
|
|
|
ENST00000283179.13:c.533G=
|
ENSP00000283179.9:p.Gly178=
|
|
ENST00000444376.6:c.533G=
|
ENSP00000393151.2:p.Gly178=
|
|
ENST00000476241.1:n.717G=
|
|
|
NM_004501.3:c.533G=
|
NP_004492.2:p.Gly178=
|
|
NM_031844.2:c.533G=
|
NP_114032.2:p.Gly178=
|
|
NM_031844.3:c.533G=
MANE Select
|
NP_114032.2:p.Gly178=
|
|