ENST00000695651.1:n.2074G>C
|
|
|
ENST00000695652.1:c.3603G>C
|
ENSP00000512083.1:p.Gln1201His
|
|
ENST00000695653.1:c.1635G>C
|
ENSP00000512084.1:p.Gln545His
|
|
ENST00000695654.1:c.2751G>C
|
ENSP00000512085.1:p.Gln917His
|
|
ENST00000695655.1:c.2667G>C
|
ENSP00000512086.1:n.2667G>C
|
|
ENST00000695692.1:n.3090G>C
|
|
|
ENST00000245907.11:c.3726G>C
MANE Select
|
ENSP00000245907.4:p.Gln1242His
|
|
ENST00000245907.10:c.3726G>C
|
ENSP00000245907.4:p.Gln1242His
|
|
ENST00000596238.1:n.169G>C
|
|
|
ENST00000601008.1:c.241+538G>C
|
ENSP00000471384.1:n.241+538G>C
|
|
NM_000064.3:c.3726G>C
|
NP_000055.2:p.Gln1242His
|
|
NM_000064.4:c.3726G>C
MANE Select
|
NP_000055.2:p.Gln1242His
|
|