ENST00000682028.1:c.-86G>T
|
ENSP00000507230.1:n.-86G>T
|
|
ENST00000682268.1:n.213G>T
|
|
|
ENST00000682902.1:n.217G>T
|
|
|
ENST00000683513.1:c.-86G>T
|
ENSP00000506809.1:n.-86G>T
|
|
ENST00000263431.4:c.-86G>T
MANE Select
|
ENSP00000263431.3:n.-86G>T
|
|
ENST00000263431.3:c.-86G>T
|
ENSP00000263431.3:n.-86G>T
|
|
ENST00000419486.1:c.-323+50G>T
|
ENSP00000387919.2:n.-323+50G>T
|
|
ENST00000474397.5:c.-322-148G>T
|
ENSP00000471271.1:n.-322-148G>T
|
|
ENST00000479081.5:c.-322-148G>T
|
ENSP00000471544.1:n.-322-148G>T
|
|
NM_001316329.1:c.-86G>T
|
NP_001303258.1:n.-86G>T
|
|
NM_002739.3:c.-86G>T , LRG_669t1:c.-86G>T
|
NP_002730.1:n.-86G>T
|
|
NM_002739.4:c.-86G>T
|
NP_002730.1:n.-86G>T
|
|
NM_002739.5:c.-86G>T
MANE Select
|
NP_002730.1:n.-86G>T
|
|
NM_001316329.2:c.-86G>T
|
NP_001303258.1:n.-86G>T
|
|