ENST00000395796.8:c.*470G>C
|
ENSP00000379142.4:n.*470G>C
|
|
ENST00000616242.5:c.472G>C
|
ENSP00000482149.2:p.Asp158His
|
|
ENST00000682635.1:n.958G>C
|
|
|
ENST00000345378.7:c.475G>C
|
ENSP00000223366.2:p.Asp159His
|
|
ENST00000403799.8:c.472G>C
MANE Select
|
ENSP00000384247.3:p.Asp158His
|
|
ENST00000671824.1:c.472G>C
|
ENSP00000500264.1:p.Asp158His
|
|
ENST00000673284.1:c.472G>C
|
ENSP00000499852.1:p.Asp158His
|
|
ENST00000345378.6:c.475G>C
|
ENSP00000223366.2:p.Asp159His
|
|
ENST00000395796.7:c.469G>C
|
ENSP00000379142.3:p.Asp157His
|
|
ENST00000403799.7:c.472G>C
|
ENSP00000384247.3:p.Asp158His
|
|
ENST00000437084.1:c.421G>C
|
ENSP00000402840.1:p.Asp141His
|
|
ENST00000616242.4:c.469G>C
|
ENSP00000482149.1:p.Asp157His
|
|
NM_000162.3:c.472G>C
|
NP_000153.1:p.Asp158His
|
|
NM_033507.1:c.475G>C
|
NP_277042.1:p.Asp159His
|
|
NM_033508.1:c.469G>C
|
NP_277043.1:p.Asp157His
|
|
NM_000162.4:c.472G>C
|
NP_000153.1:p.Asp158His
|
|
NM_001354800.1:c.472G>C
|
NP_001341729.1:p.Asp158His
|
|
NM_033507.2:c.475G>C
|
NP_277042.1:p.Asp159His
|
|
NM_033508.2:c.469G>C
|
NP_277043.1:p.Asp157His
|
|
NM_000162.5:c.472G>C
MANE Select
|
NP_000153.1:p.Asp158His
|
|
NM_033507.3:c.475G>C
|
NP_277042.1:p.Asp159His
|
|
NM_033508.3:c.469G>C
|
NP_277043.1:p.Asp157His
|
|