ENST00000695651.1:n.916G>C
|
|
|
ENST00000695652.1:c.2445G>C
|
ENSP00000512083.1:p.Gln815His
|
|
ENST00000695653.1:c.477G>C
|
ENSP00000512084.1:p.Gln159His
|
|
ENST00000695654.1:c.1692G>C
|
ENSP00000512085.1:p.Gln564His
|
|
ENST00000695655.1:c.1509G>C
|
ENSP00000512086.1:n.1509G>C
|
|
ENST00000695692.1:n.1932G>C
|
|
|
ENST00000245907.11:c.2568G>C
MANE Select
|
ENSP00000245907.4:p.Gln856His
|
|
ENST00000245907.10:c.2568G>C
|
ENSP00000245907.4:p.Gln856His
|
|
ENST00000594005.1:n.49G>C
|
|
|
ENST00000602053.1:n.616G>C
|
|
|
NM_000064.3:c.2568G>C
|
NP_000055.2:p.Gln856His
|
|
NM_000064.4:c.2568G>C
MANE Select
|
NP_000055.2:p.Gln856His
|
|