|
NM_006767.4:c.1682G>A
MANE Select
|
NP_006758.2:p.Arg561His
|
|
ENST00000646124.2:c.1682G>A
MANE Select
|
ENSP00000496779.1:p.Arg561His
|
|
NM_006767.3:c.1682G>A
|
NP_006758.2:p.Arg561His
|
|
ENST00000215739.12:c.1682G>A
|
ENSP00000215739.8:p.Arg561His
|
|
ENST00000415354.6:c.44-50G>A
|
ENSP00000393765.2:n.44-50G>A
|
|
ENST00000415817.2:c.39G>A
|
|
|
ENST00000479606.5:n.1828G>A
|
|
|
ENST00000491432.5:n.148G>A
|
|
|
ENST00000495142.5:n.298G>A
|
|
|
ENST00000495142.6:n.1315G>A
|
|
|
ENST00000642151.1:c.1513G>A
|
|
|
ENST00000643578.1:n.1704G>A
|
|
|
ENST00000643710.1:n.543G>A
|
|
|
ENST00000646506.1:n.1549G>A
|
|
|
ENST00000700578.1:c.1682G>A
|
ENSP00000515073.1:p.Arg561His
|