ENST00000682114.1:c.450-1G>T
|
ENSP00000507245.1:n.450-1G>T
|
|
ENST00000682478.1:n.640-1G>T
|
|
|
ENST00000683576.1:n.640-1G>T
|
|
|
ENST00000683627.1:c.450-1G>T
|
ENSP00000507533.1:n.450-1G>T
|
|
ENST00000684082.1:c.407-1G>T
|
ENSP00000508266.1:n.407-1G>T
|
|
ENST00000684633.1:n.422-1G>T
|
|
|
ENST00000684678.1:c.446-1G>T
|
ENSP00000507059.1:n.446-1G>T
|
|
ENST00000369842.9:c.450-1G>T
MANE Select
|
ENSP00000358857.4:n.450-1G>T
|
|
ENST00000369835.3:c.345-1G>T
|
ENSP00000358850.3:n.345-1G>T
|
|
ENST00000369842.8:c.450-1G>T
|
ENSP00000358857.4:n.450-1G>T
|
|
ENST00000428228.5:c.*355-1G>T
|
ENSP00000401081.1:n.*355-1G>T
|
|
ENST00000468294.5:n.488G>T
|
|
|
ENST00000471965.1:n.239-1G>T
|
|
|
ENST00000485261.1:n.718G>T
|
|
|
ENST00000486738.5:n.886G>T
|
|
|
ENST00000492448.1:n.433-1G>T
|
|
|
NM_000117.2:c.450-1G>T , LRG_745t1:c.450-1G>T
|
NP_000108.1:n.450-1G>T
|
|
XM_024452349.1:c.456-1G>T
|
XP_024308117.1:n.456-1G>T
|
|
NM_000117.3:c.450-1G>T
MANE Select
|
NP_000108.1:n.450-1G>T
|
|