ENST00000695651.1:n.997G>T
|
|
|
ENST00000695652.1:c.2526G>T
|
ENSP00000512083.1:p.Gln842His
|
|
ENST00000695653.1:c.558G>T
|
ENSP00000512084.1:p.Gln186His
|
|
ENST00000695654.1:c.1773G>T
|
ENSP00000512085.1:p.Gln591His
|
|
ENST00000695655.1:c.1590G>T
|
ENSP00000512086.1:n.1590G>T
|
|
ENST00000695692.1:n.2013G>T
|
|
|
ENST00000245907.11:c.2649G>T
MANE Select
|
ENSP00000245907.4:p.Gln883His
|
|
ENST00000245907.10:c.2649G>T
|
ENSP00000245907.4:p.Gln883His
|
|
ENST00000594005.1:n.225G>T
|
|
|
NM_000064.3:c.2649G>T
|
NP_000055.2:p.Gln883His
|
|
NM_000064.4:c.2649G>T
MANE Select
|
NP_000055.2:p.Gln883His
|
|