ENST00000336906.6:c.194G=
MANE Select
|
ENSP00000338082.4:p.Gly65=
|
|
ENST00000380252.6:c.29G=
|
ENSP00000369602.2:p.Gly10=
|
|
ENST00000380259.7:c.1740G=
|
ENSP00000369609.3:n.1740G=
|
|
ENST00000642908.1:c.194G=
|
ENSP00000495346.1:p.Gly65=
|
|
ENST00000647543.1:c.194G=
|
ENSP00000496470.1:p.Gly65=
|
|
ENST00000336906.4:c.194G=
|
ENSP00000338082.4:p.Gly65=
|
|
ENST00000380252.5:c.164G=
|
ENSP00000369602.1:p.Gly55=
|
|
ENST00000380259.6:c.194G=
|
ENSP00000369609.2:p.Gly65=
|
|
ENST00000444587.1:c.*63G=
|
ENSP00000488218.1:n.*63G=
|
|
ENST00000620888.4:c.194G=
|
ENSP00000479637.1:p.Gly65=
|
|
ENST00000624109.1:c.161C=
|
ENSP00000485458.1:p.Ala54=
|
|
NM_000184.2:c.194G=
|
NP_000175.1:p.Gly65=
|
|
NM_000184.3:c.194G=
MANE Select
|
NP_000175.1:p.Gly65=
|
|