ENST00000682850.1:c.-332G>A
MANE Select
|
ENSP00000508024.1:n.-332G>A
|
|
ENST00000558573.1:n.219G>A
|
|
|
XM_011521338.1:c.-332G>A
|
XP_011519640.1:n.-332G>A
|
|
XM_011521339.1:c.-213G>A
|
XP_011519641.1:n.-213G>A
|
|
XM_011521340.1:c.-154G>A
|
XP_011519642.1:n.-154G>A
|
|
XM_011521343.1:c.-416G>A
|
XP_011519645.1:n.-416G>A
|
|
XM_011521345.1:c.-387G>A
|
XP_011519647.1:n.-387G>A
|
|
XM_011521338.3:c.-332G>A
|
XP_011519640.1:n.-332G>A
|
|
XM_011521339.3:c.-213G>A
|
XP_011519641.1:n.-213G>A
|
|
XM_011521340.3:c.-154G>A
|
XP_011519642.1:n.-154G>A
|
|
XM_011521343.3:c.-416G>A
|
XP_011519645.1:n.-416G>A
|
|
XM_011521345.3:c.-387G>A
|
XP_011519647.1:n.-387G>A
|
|
NM_001387260.1:c.-76+234G>A
|
NP_001374189.1:n.-76+234G>A
|
|
NM_001387261.1:c.-154G>A
|
NP_001374190.1:n.-154G>A
|
|
NM_001387262.1:c.-422G>A
|
NP_001374191.1:n.-422G>A
|
|
NM_001387263.1:c.-332G>A
MANE Select
|
NP_001374192.1:n.-332G>A
|
|