ENST00000695651.1:n.1115G>C
|
|
|
ENST00000695652.1:c.2644G>C
|
ENSP00000512083.1:p.Asp882His
|
|
ENST00000695653.1:c.676G>C
|
ENSP00000512084.1:p.Asp226His
|
|
ENST00000695654.1:c.1891G>C
|
ENSP00000512085.1:p.Asp631His
|
|
ENST00000695655.1:c.1708G>C
|
ENSP00000512086.1:n.1708G>C
|
|
ENST00000695692.1:n.2131G>C
|
|
|
ENST00000245907.11:c.2767G>C
MANE Select
|
ENSP00000245907.4:p.Asp923His
|
|
ENST00000245907.10:c.2767G>C
|
ENSP00000245907.4:p.Asp923His
|
|
ENST00000594005.1:n.343G>C
|
|
|
NM_000064.3:c.2767G>C
|
NP_000055.2:p.Asp923His
|
|
NM_000064.4:c.2767G>C
MANE Select
|
NP_000055.2:p.Asp923His
|
|