ENST00000682850.1:c.-367T>G
MANE Select
|
ENSP00000508024.1:n.-367T>G
|
|
ENST00000558573.1:n.184T>G
|
|
|
XM_011521338.1:c.-367T>G
|
XP_011519640.1:n.-367T>G
|
|
XM_011521339.1:c.-248T>G
|
XP_011519641.1:n.-248T>G
|
|
XM_011521340.1:c.-189T>G
|
XP_011519642.1:n.-189T>G
|
|
XM_011521343.1:c.-451T>G
|
XP_011519645.1:n.-451T>G
|
|
XM_011521345.1:c.-422T>G
|
XP_011519647.1:n.-422T>G
|
|
XM_011521338.3:c.-367T>G
|
XP_011519640.1:n.-367T>G
|
|
XM_011521339.3:c.-248T>G
|
XP_011519641.1:n.-248T>G
|
|
XM_011521340.3:c.-189T>G
|
XP_011519642.1:n.-189T>G
|
|
XM_011521343.3:c.-451T>G
|
XP_011519645.1:n.-451T>G
|
|
XM_011521345.3:c.-422T>G
|
XP_011519647.1:n.-422T>G
|
|
NM_001387260.1:c.-76+199T>G
|
NP_001374189.1:n.-76+199T>G
|
|
NM_001387261.1:c.-189T>G
|
NP_001374190.1:n.-189T>G
|
|
NM_001387262.1:c.-457T>G
|
NP_001374191.1:n.-457T>G
|
|
NM_001387263.1:c.-367T>G
MANE Select
|
NP_001374192.1:n.-367T>G
|
|