ENST00000578493.2:n.699-8G>T
|
|
|
ENST00000699291.1:c.491-8G>T
|
ENSP00000514272.1:n.491-8G>T
|
|
ENST00000699292.1:n.398G>T
|
|
|
ENST00000225275.4:c.1366-8G>T
MANE Select
|
ENSP00000225275.3:n.1366-8G>T
|
|
ENST00000225275.3:c.1366-8G>T
|
ENSP00000225275.3:n.1366-8G>T
|
|
NM_000250.1:c.1366-8G>T , LRG_84t1:c.1366-8G>T
|
NP_000241.1:n.1366-8G>T
|
|
XM_011524821.1:c.1552-8G>T
|
XP_011523123.1:n.1552-8G>T
|
|
XM_011524822.1:c.1081-8G>T
|
XP_011523124.1:n.1081-8G>T
|
|
XM_011524823.1:c.1391-8G>T
|
XP_011523125.1:n.1391-8G>T
|
|
NM_000250.2:c.1366-8G>T
MANE Select
|
NP_000241.1:n.1366-8G>T
|
|