ENST00000298296.1:c.1076G>T
MANE Select
|
ENSP00000298296.1:p.Gly359Val
|
|
ENST00000443323.2:c.-118-919G>T
|
ENSP00000438254.1:n.-118-919G>T
|
|
ENST00000483584.5:n.288+105G>T
|
|
|
ENST00000544766.5:c.-240+105G>T
|
ENSP00000440444.1:n.-240+105G>T
|
|
NM_138702.1:c.1076G>T
MANE Select
|
NP_619647.1:p.Gly359Val
|
|
NM_177456.2:c.-240+105G>T
|
NP_803251.1:n.-240+105G>T
|
|
XM_011531267.1:c.-163+105G>T
|
XP_011529569.1:n.-163+105G>T
|
|
XM_011531267.3:c.-163+105G>T
|
XP_011529569.1:n.-163+105G>T
|
|
XM_017029265.2:c.-240+105G>T
|
XP_016884754.1:n.-240+105G>T
|
|