ENST00000398752.11:c.620G>A
MANE Select
|
ENSP00000381736.5:p.Arg207His
|
|
ENST00000282050.6:c.620G>A
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ENSP00000282050.2:p.Arg207His
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|
ENST00000398752.10:c.620G>A
|
ENSP00000381736.5:p.Arg207His
|
|
ENST00000586592.5:c.*683G>A
|
ENSP00000466275.3:n.*683G>A
|
|
ENST00000589252.5:c.353G>A
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ENSP00000466975.1:p.Arg118His
|
|
ENST00000589611.1:n.828G>A
|
|
|
ENST00000589869.5:c.470G>A
|
ENSP00000465497.1:p.Arg157His
|
|
ENST00000590156.5:c.*516G>A
|
ENSP00000466309.1:n.*516G>A
|
|
ENST00000590665.5:c.554G>A
|
ENSP00000467037.1:p.Arg185His
|
|
ENST00000592364.5:c.226+2169G>A
|
ENSP00000468618.1:n.226+2169G>A
|
|
ENST00000593152.6:c.470G>A
|
ENSP00000465477.2:p.Arg157His
|
|
NM_001001935.2:c.470G>A
|
NP_001001935.1:p.Arg157His
|
|
NM_001001937.1:c.620G>A
|
NP_001001937.1:p.Arg207His
|
|
NM_001257334.1:c.554G>A
|
NP_001244263.1:p.Arg185His
|
|
NM_001257335.1:c.470G>A
|
NP_001244264.1:p.Arg157His
|
|
NM_004046.5:c.620G>A
|
NP_004037.1:p.Arg207His
|
|
XM_011526018.1:c.470G>A
|
XP_011524320.1:p.Arg157His
|
|
XM_017025789.1:c.620G>A
|
XP_016881278.1:p.Arg207His
|
|
NM_004046.6:c.620G>A
MANE Select
|
NP_004037.1:p.Arg207His
|
|
NM_001001935.3:c.470G>A
|
NP_001001935.1:p.Arg157His
|
|
NM_001257334.2:c.554G>A
|
NP_001244263.1:p.Arg185His
|
|
NM_001001937.2:c.620G>A
|
NP_001001937.1:p.Arg207His
|
|
NM_001257335.2:c.470G>A
|
NP_001244264.1:p.Arg157His
|
|