|
NM_006767.4:c.994-2A>T
MANE Select
|
NP_006758.2:n.994-2A>T
|
|
ENST00000646124.2:c.994-2A>T
MANE Select
|
ENSP00000496779.1:n.994-2A>T
|
|
NM_006767.3:c.994-2A>T
|
NP_006758.2:n.994-2A>T
|
|
ENST00000215739.12:c.994-2A>T
|
ENSP00000215739.8:n.994-2A>T
|
|
ENST00000461510.1:n.95-2A>T
|
|
|
ENST00000479606.5:n.1140-2A>T
|
|
|
ENST00000492480.1:n.50-2A>T
|
|
|
ENST00000495142.6:n.339-2A>T
|
|
|
ENST00000497716.5:n.821-2A>T
|
|
|
ENST00000642151.1:c.825-2A>T
|
|
|
ENST00000643578.1:n.1016-2A>T
|
|
|
ENST00000646506.1:n.573-2A>T
|
|
|
ENST00000700578.1:c.994-2A>T
|
ENSP00000515073.1:n.994-2A>T
|