ENST00000695651.1:n.2012G>C
|
|
|
ENST00000695652.1:c.3541G>C
|
ENSP00000512083.1:p.Asp1181His
|
|
ENST00000695653.1:c.1573G>C
|
ENSP00000512084.1:p.Asp525His
|
|
ENST00000695654.1:c.2689G>C
|
ENSP00000512085.1:p.Asp897His
|
|
ENST00000695655.1:c.2605G>C
|
ENSP00000512086.1:n.2605G>C
|
|
ENST00000695692.1:n.3028G>C
|
|
|
ENST00000245907.11:c.3664G>C
MANE Select
|
ENSP00000245907.4:p.Asp1222His
|
|
ENST00000245907.10:c.3664G>C
|
ENSP00000245907.4:p.Asp1222His
|
|
ENST00000596238.1:n.107G>C
|
|
|
ENST00000601008.1:c.241+476G>C
|
ENSP00000471384.1:n.241+476G>C
|
|
NM_000064.3:c.3664G>C
|
NP_000055.2:p.Asp1222His
|
|
NM_000064.4:c.3664G>C
MANE Select
|
NP_000055.2:p.Asp1222His
|
|