ENST00000298296.1:c.1068G>T
MANE Select
|
ENSP00000298296.1:p.Gln356His
|
|
ENST00000443323.2:c.-118-927G>T
|
ENSP00000438254.1:n.-118-927G>T
|
|
ENST00000483584.5:n.288+97G>T
|
|
|
ENST00000544766.5:c.-240+97G>T
|
ENSP00000440444.1:n.-240+97G>T
|
|
NM_138702.1:c.1068G>T
MANE Select
|
NP_619647.1:p.Gln356His
|
|
NM_177456.2:c.-240+97G>T
|
NP_803251.1:n.-240+97G>T
|
|
XM_011531267.1:c.-163+97G>T
|
XP_011529569.1:n.-163+97G>T
|
|
XM_011531267.3:c.-163+97G>T
|
XP_011529569.1:n.-163+97G>T
|
|
XM_017029265.2:c.-240+97G>T
|
XP_016884754.1:n.-240+97G>T
|
|