ENST00000321612.8:c.2010G>A
MANE Select
|
ENSP00000370737.4:p.Val670=
|
|
ENST00000460457.2:n.170G>A
|
|
|
ENST00000638233.1:n.445G>A
|
|
|
ENST00000638661.1:c.210G>A
|
ENSP00000491369.1:p.Val70=
|
|
ENST00000638694.1:n.197G>A
|
|
|
ENST00000639318.1:c.210G>A
|
ENSP00000491932.1:p.Val70=
|
|
ENST00000639364.1:n.1710G>A
|
|
|
ENST00000639443.1:n.1578G>A
|
|
|
ENST00000639954.1:n.1718G>A
|
|
|
ENST00000640208.1:c.210G>A
|
ENSP00000491895.1:p.Val70=
|
|
ENST00000640505.1:n.249G>A
|
|
|
ENST00000640592.1:n.1893G>A
|
|
|
ENST00000321612.6:c.2010G>A
|
ENSP00000370737.3:p.Val670=
|
|
ENST00000460457.1:n.149G>A
|
|
|
NM_000170.2:c.2010G>A , LRG_643t1:c.2010G>A
|
NP_000161.2:p.Val670=
|
|
NM_000170.3:c.2010G>A
MANE Select
|
NP_000161.2:p.Val670=
|
|