ENST00000682850.1:c.-356G>T
MANE Select
|
ENSP00000508024.1:n.-356G>T
|
|
ENST00000558573.1:n.195G>T
|
|
|
XM_011521338.1:c.-356G>T
|
XP_011519640.1:n.-356G>T
|
|
XM_011521339.1:c.-237G>T
|
XP_011519641.1:n.-237G>T
|
|
XM_011521340.1:c.-178G>T
|
XP_011519642.1:n.-178G>T
|
|
XM_011521343.1:c.-440G>T
|
XP_011519645.1:n.-440G>T
|
|
XM_011521345.1:c.-411G>T
|
XP_011519647.1:n.-411G>T
|
|
XM_011521338.3:c.-356G>T
|
XP_011519640.1:n.-356G>T
|
|
XM_011521339.3:c.-237G>T
|
XP_011519641.1:n.-237G>T
|
|
XM_011521340.3:c.-178G>T
|
XP_011519642.1:n.-178G>T
|
|
XM_011521343.3:c.-440G>T
|
XP_011519645.1:n.-440G>T
|
|
XM_011521345.3:c.-411G>T
|
XP_011519647.1:n.-411G>T
|
|
NM_001387260.1:c.-76+210G>T
|
NP_001374189.1:n.-76+210G>T
|
|
NM_001387261.1:c.-178G>T
|
NP_001374190.1:n.-178G>T
|
|
NM_001387262.1:c.-446G>T
|
NP_001374191.1:n.-446G>T
|
|
NM_001387263.1:c.-356G>T
MANE Select
|
NP_001374192.1:n.-356G>T
|
|