|
NM_006767.4:c.2325+1G>A
MANE Select
|
NP_006758.2:n.2325+1G>A
|
|
ENST00000646124.2:c.2325+1G>A
MANE Select
|
ENSP00000496779.1:n.2325+1G>A
|
|
NM_006767.3:c.2325+1G>A
|
NP_006758.2:n.2325+1G>A
|
|
ENST00000215739.12:c.2325+1G>A
|
ENSP00000215739.8:n.2325+1G>A
|
|
ENST00000415817.1:c.223+1G>A
|
|
|
ENST00000415817.2:c.754+1G>A
|
|
|
ENST00000452988.5:c.487+1G>A
|
ENSP00000408789.1:n.487+1G>A
|
|
ENST00000463909.1:n.1623+1G>A
|
|
|
ENST00000479606.5:n.2471+1G>A
|
|
|
ENST00000495142.6:n.2677+1G>A
|
|
|
ENST00000498649.1:n.342G>A
|
|
|
ENST00000642151.1:c.2156+1G>A
|
|
|
ENST00000643578.1:n.2347+1G>A
|
|
|
ENST00000643710.1:n.1186+1G>A
|
|
|
ENST00000646506.1:n.2192+1G>A
|
|
|
ENST00000700578.1:c.2325+1G>A
|
ENSP00000515073.1:n.2325+1G>A
|