ENST00000298296.1:c.1107A>G
MANE Select
|
ENSP00000298296.1:p.Gln369=
|
|
ENST00000443323.2:c.-118-888A>G
|
ENSP00000438254.1:n.-118-888A>G
|
|
ENST00000483584.5:n.288+136A>G
|
|
|
ENST00000544766.5:c.-240+136A>G
|
ENSP00000440444.1:n.-240+136A>G
|
|
NM_138702.1:c.1107A>G
MANE Select
|
NP_619647.1:p.Gln369=
|
|
NM_177456.2:c.-240+136A>G
|
NP_803251.1:n.-240+136A>G
|
|
XM_011531267.1:c.-163+136A>G
|
XP_011529569.1:n.-163+136A>G
|
|
XM_011531267.3:c.-163+136A>G
|
XP_011529569.1:n.-163+136A>G
|
|
XM_017029265.2:c.-240+136A>G
|
XP_016884754.1:n.-240+136A>G
|
|