ENST00000695651.1:n.2125G>T
|
|
|
ENST00000695652.1:c.3654G>T
|
ENSP00000512083.1:p.Gln1218His
|
|
ENST00000695653.1:c.1686G>T
|
ENSP00000512084.1:p.Gln562His
|
|
ENST00000695654.1:c.2802G>T
|
ENSP00000512085.1:p.Gln934His
|
|
ENST00000695655.1:c.2718G>T
|
ENSP00000512086.1:n.2718G>T
|
|
ENST00000695692.1:n.3141G>T
|
|
|
ENST00000245907.11:c.3777G>T
MANE Select
|
ENSP00000245907.4:p.Gln1259His
|
|
ENST00000245907.10:c.3777G>T
|
ENSP00000245907.4:p.Gln1259His
|
|
ENST00000596238.1:n.220G>T
|
|
|
ENST00000601008.1:c.241+589G>T
|
ENSP00000471384.1:n.241+589G>T
|
|
NM_000064.3:c.3777G>T
|
NP_000055.2:p.Gln1259His
|
|
NM_000064.4:c.3777G>T
MANE Select
|
NP_000055.2:p.Gln1259His
|
|