ENST00000321612.8:c.1914G=
MANE Select
|
ENSP00000370737.4:p.Glu638=
|
|
ENST00000460457.2:n.74G=
|
|
|
ENST00000638233.1:n.349G=
|
|
|
ENST00000638661.1:c.114G=
|
ENSP00000491369.1:p.Glu38=
|
|
ENST00000638694.1:n.101G=
|
|
|
ENST00000639318.1:c.114G=
|
ENSP00000491932.1:p.Glu38=
|
|
ENST00000639364.1:n.1614G=
|
|
|
ENST00000639443.1:n.1482G=
|
|
|
ENST00000639954.1:n.1622G=
|
|
|
ENST00000640208.1:c.114G=
|
ENSP00000491895.1:p.Glu38=
|
|
ENST00000640505.1:n.153G=
|
|
|
ENST00000640592.1:n.1797G=
|
|
|
ENST00000321612.6:c.1914G=
|
ENSP00000370737.3:p.Glu638=
|
|
ENST00000460457.1:n.53G=
|
|
|
NM_000170.2:c.1914G= , LRG_643t1:c.1914G=
|
NP_000161.2:p.Glu638=
|
|
NM_000170.3:c.1914G=
MANE Select
|
NP_000161.2:p.Glu638=
|
|