ENST00000682850.1:c.-348G>C
MANE Select
|
ENSP00000508024.1:n.-348G>C
|
|
ENST00000558573.1:n.203G>C
|
|
|
XM_011521338.1:c.-348G>C
|
XP_011519640.1:n.-348G>C
|
|
XM_011521339.1:c.-229G>C
|
XP_011519641.1:n.-229G>C
|
|
XM_011521340.1:c.-170G>C
|
XP_011519642.1:n.-170G>C
|
|
XM_011521343.1:c.-432G>C
|
XP_011519645.1:n.-432G>C
|
|
XM_011521345.1:c.-403G>C
|
XP_011519647.1:n.-403G>C
|
|
XM_011521338.3:c.-348G>C
|
XP_011519640.1:n.-348G>C
|
|
XM_011521339.3:c.-229G>C
|
XP_011519641.1:n.-229G>C
|
|
XM_011521340.3:c.-170G>C
|
XP_011519642.1:n.-170G>C
|
|
XM_011521343.3:c.-432G>C
|
XP_011519645.1:n.-432G>C
|
|
XM_011521345.3:c.-403G>C
|
XP_011519647.1:n.-403G>C
|
|
NM_001387260.1:c.-76+218G>C
|
NP_001374189.1:n.-76+218G>C
|
|
NM_001387261.1:c.-170G>C
|
NP_001374190.1:n.-170G>C
|
|
NM_001387262.1:c.-438G>C
|
NP_001374191.1:n.-438G>C
|
|
NM_001387263.1:c.-348G>C
MANE Select
|
NP_001374192.1:n.-348G>C
|
|