|
NM_006767.4:c.1785+1G>A
MANE Select
|
NP_006758.2:n.1785+1G>A
|
|
ENST00000646124.2:c.1785+1G>A
MANE Select
|
ENSP00000496779.1:n.1785+1G>A
|
|
NM_006767.3:c.1785+1G>A
|
NP_006758.2:n.1785+1G>A
|
|
ENST00000215739.12:c.1785+1G>A
|
ENSP00000215739.8:n.1785+1G>A
|
|
ENST00000415354.6:c.97+1G>A
|
ENSP00000393765.2:n.97+1G>A
|
|
ENST00000415817.2:c.142+1G>A
|
|
|
ENST00000439171.5:c.67+1G>A
|
|
|
ENST00000464807.1:n.46+1G>A
|
|
|
ENST00000479606.5:n.1931+1G>A
|
|
|
ENST00000491432.5:n.251+1G>A
|
|
|
ENST00000495142.5:n.401+1G>A
|
|
|
ENST00000495142.6:n.1418+1G>A
|
|
|
ENST00000642151.1:c.1616+1G>A
|
|
|
ENST00000643578.1:n.1807+1G>A
|
|
|
ENST00000643710.1:n.646+1G>A
|
|
|
ENST00000646506.1:n.1652+1G>A
|
|
|
ENST00000700578.1:c.1785+1G>A
|
ENSP00000515073.1:n.1785+1G>A
|