|
NM_006767.4:c.1806G>A
MANE Select
|
NP_006758.2:p.Val602=
|
|
ENST00000646124.2:c.1806G>A
MANE Select
|
ENSP00000496779.1:p.Val602=
|
|
NM_006767.3:c.1806G>A
|
NP_006758.2:p.Val602=
|
|
ENST00000215739.12:c.1806G>A
|
ENSP00000215739.8:p.Val602=
|
|
ENST00000415354.6:c.118G>A
|
ENSP00000393765.2:p.Gly40Ser
|
|
ENST00000415817.2:c.143-25G>A
|
|
|
ENST00000439171.5:c.88G>A
|
|
|
ENST00000464807.1:n.67G>A
|
|
|
ENST00000479606.5:n.1952G>A
|
|
|
ENST00000491432.5:n.252-25G>A
|
|
|
ENST00000495142.5:n.422G>A
|
|
|
ENST00000495142.6:n.1439G>A
|
|
|
ENST00000642151.1:c.1637G>A
|
|
|
ENST00000643578.1:n.1828G>A
|
|
|
ENST00000643710.1:n.667G>A
|
|
|
ENST00000646506.1:n.1673G>A
|
|
|
ENST00000700578.1:c.1806G>A
|
ENSP00000515073.1:p.Val602=
|