ENST00000321612.8:c.2182G=
MANE Select
|
ENSP00000370737.4:p.Gly728=
|
|
ENST00000638233.1:n.617G=
|
|
|
ENST00000638661.1:c.382G=
|
ENSP00000491369.1:p.Gly128=
|
|
ENST00000638694.1:n.369G=
|
|
|
ENST00000639318.1:c.382G=
|
ENSP00000491932.1:p.Gly128=
|
|
ENST00000639364.1:n.1882G=
|
|
|
ENST00000639443.1:n.1750G=
|
|
|
ENST00000639954.1:n.1890G=
|
|
|
ENST00000640505.1:n.421G=
|
|
|
ENST00000321612.6:c.2182G=
|
ENSP00000370737.3:p.Gly728=
|
|
NM_000170.2:c.2182G= , LRG_643t1:c.2182G=
|
NP_000161.2:p.Gly728=
|
|
NM_000170.3:c.2182G=
MANE Select
|
NP_000161.2:p.Gly728=
|
|