ENST00000321612.8:c.2005G=
MANE Select
|
ENSP00000370737.4:p.Glu669=
|
|
ENST00000460457.2:n.165G=
|
|
|
ENST00000638233.1:n.440G=
|
|
|
ENST00000638661.1:c.205G=
|
ENSP00000491369.1:p.Glu69=
|
|
ENST00000638694.1:n.192G=
|
|
|
ENST00000639318.1:c.205G=
|
ENSP00000491932.1:p.Glu69=
|
|
ENST00000639364.1:n.1705G=
|
|
|
ENST00000639443.1:n.1573G=
|
|
|
ENST00000639954.1:n.1713G=
|
|
|
ENST00000640208.1:c.205G=
|
ENSP00000491895.1:p.Glu69=
|
|
ENST00000640505.1:n.244G=
|
|
|
ENST00000640592.1:n.1888G=
|
|
|
ENST00000321612.6:c.2005G=
|
ENSP00000370737.3:p.Glu669=
|
|
ENST00000460457.1:n.144G=
|
|
|
NM_000170.2:c.2005G= , LRG_643t1:c.2005G=
|
NP_000161.2:p.Glu669=
|
|
NM_000170.3:c.2005G=
MANE Select
|
NP_000161.2:p.Glu669=
|
|