ENST00000695651.1:n.993A>G
|
|
|
ENST00000695652.1:c.2522A>G
|
ENSP00000512083.1:p.His841Arg
|
|
ENST00000695653.1:c.554A>G
|
ENSP00000512084.1:p.His185Arg
|
|
ENST00000695654.1:c.1769A>G
|
ENSP00000512085.1:p.His590Arg
|
|
ENST00000695655.1:c.1586A>G
|
ENSP00000512086.1:n.1586A>G
|
|
ENST00000695692.1:n.2009A>G
|
|
|
ENST00000245907.11:c.2645A>G
MANE Select
|
ENSP00000245907.4:p.His882Arg
|
|
ENST00000245907.10:c.2645A>G
|
ENSP00000245907.4:p.His882Arg
|
|
ENST00000594005.1:n.221A>G
|
|
|
NM_000064.3:c.2645A>G
|
NP_000055.2:p.His882Arg
|
|
NM_000064.4:c.2645A>G
MANE Select
|
NP_000055.2:p.His882Arg
|
|