|
NM_006767.4:c.1353+1G>T
MANE Select
|
NP_006758.2:n.1353+1G>T
|
|
ENST00000646124.2:c.1353+1G>T
MANE Select
|
ENSP00000496779.1:n.1353+1G>T
|
|
NM_006767.3:c.1353+1G>T
|
NP_006758.2:n.1353+1G>T
|
|
ENST00000215739.12:c.1353+1G>T
|
ENSP00000215739.8:n.1353+1G>T
|
|
ENST00000479606.5:n.1499+1G>T
|
|
|
ENST00000492480.1:n.402+1G>T
|
|
|
ENST00000495142.6:n.698+1G>T
|
|
|
ENST00000642151.1:c.1184+1G>T
|
|
|
ENST00000643578.1:n.1375+1G>T
|
|
|
ENST00000643710.1:n.214+1G>T
|
|
|
ENST00000646506.1:n.932+1G>T
|
|
|
ENST00000700578.1:c.1353+1G>T
|
ENSP00000515073.1:n.1353+1G>T
|