ENST00000682850.1:c.-437G>T
MANE Select
|
ENSP00000508024.1:n.-437G>T
|
|
ENST00000558573.1:n.114G>T
|
|
|
XM_011521338.1:c.-437G>T
|
XP_011519640.1:n.-437G>T
|
|
XM_011521339.1:c.-318G>T
|
XP_011519641.1:n.-318G>T
|
|
XM_011521340.1:c.-259G>T
|
XP_011519642.1:n.-259G>T
|
|
XM_011521343.1:c.-521G>T
|
XP_011519645.1:n.-521G>T
|
|
XM_011521345.1:c.-492G>T
|
XP_011519647.1:n.-492G>T
|
|
XM_011521338.3:c.-437G>T
|
XP_011519640.1:n.-437G>T
|
|
XM_011521339.3:c.-318G>T
|
XP_011519641.1:n.-318G>T
|
|
XM_011521340.3:c.-259G>T
|
XP_011519642.1:n.-259G>T
|
|
XM_011521343.3:c.-521G>T
|
XP_011519645.1:n.-521G>T
|
|
XM_011521345.3:c.-492G>T
|
XP_011519647.1:n.-492G>T
|
|
NM_001387260.1:c.-76+129G>T
|
NP_001374189.1:n.-76+129G>T
|
|
NM_001387261.1:c.-259G>T
|
NP_001374190.1:n.-259G>T
|
|
NM_001387262.1:c.-527G>T
|
NP_001374191.1:n.-527G>T
|
|
NM_001387263.1:c.-437G>T
MANE Select
|
NP_001374192.1:n.-437G>T
|
|