|
NM_006767.4:c.651+1G>A
MANE Select
|
NP_006758.2:n.651+1G>A
|
|
ENST00000646124.2:c.651+1G>A
MANE Select
|
ENSP00000496779.1:n.651+1G>A
|
|
NM_006767.3:c.651+1G>A
|
NP_006758.2:n.651+1G>A
|
|
ENST00000215739.12:c.651+1G>A
|
ENSP00000215739.8:n.651+1G>A
|
|
ENST00000414985.5:c.*217+1G>A
|
ENSP00000397247.1:n.*217+1G>A
|
|
ENST00000479606.5:n.797+1G>A
|
|
|
ENST00000480895.1:n.347+1G>A
|
|
|
ENST00000497716.5:n.34+1G>A
|
|
|
ENST00000642151.1:c.482+1G>A
|
|
|
ENST00000644435.1:c.473+1G>A
|
|
|
ENST00000646506.1:n.230+1G>A
|
|
|
ENST00000700578.1:c.651+1G>A
|
ENSP00000515073.1:n.651+1G>A
|