ENST00000403729.7:c.-199G>A
MANE Select
|
ENSP00000385575.2:n.-199G>A
|
|
ENST00000679571.1:c.-130G>A
|
ENSP00000506307.1:n.-130G>A
|
|
ENST00000681115.1:c.-199G>A
|
ENSP00000505618.1:n.-199G>A
|
|
ENST00000681710.1:c.-130G>A
|
ENSP00000505865.1:n.-130G>A
|
|
ENST00000403729.6:c.-199G>A
|
ENSP00000385575.2:n.-199G>A
|
|
ENST00000404191.5:c.-80+636G>A
|
ENSP00000384028.1:n.-80+636G>A
|
|
ENST00000506286.1:n.630-1105G>A
|
|
|
ENST00000514959.1:n.248+6594G>A
|
|
|
NM_001145794.1:c.-199G>A
|
NP_001139266.1:n.-199G>A
|
|
NM_001286780.1:c.-80+636G>A
|
NP_001273709.1:n.-80+636G>A
|
|
NM_001286781.1:c.-130G>A
|
NP_001273710.1:n.-130G>A
|
|
NM_058172.5:c.-199G>A
|
NP_477520.2:n.-199G>A
|
|
XM_011531587.1:c.-80+636G>A
|
XP_011529889.1:n.-80+636G>A
|
|
XM_011531587.3:c.-80+636G>A
|
XP_011529889.1:n.-80+636G>A
|
|
NM_058172.6:c.-199G>A
MANE Select
|
NP_477520.2:n.-199G>A
|
|
NM_001286780.2:c.-80+636G>A
|
NP_001273709.1:n.-80+636G>A
|
|
NM_001286781.2:c.-130G>A
|
NP_001273710.1:n.-130G>A
|
|
NM_001145794.2:c.-199G>A
|
NP_001139266.1:n.-199G>A
|
|