ENST00000324444.9:c.745T>A
MANE Select
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ENSP00000316130.3:p.Trp249Arg
|
|
ENST00000397428.8:c.67-1108T>A
|
|
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ENST00000465425.2:n.857T>A
|
|
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ENST00000324444.7:c.745T>A
|
ENSP00000316130.3:p.Trp249Arg
|
|
ENST00000340477.9:c.406T>A
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ENSP00000343152.5:p.Trp136Arg
|
|
ENST00000397428.7:c.40-1108T>A
|
ENSP00000380572.3:n.40-1108T>A
|
|
ENST00000465425.1:n.857T>A
|
|
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ENST00000490730.1:c.688+57T>A
|
ENSP00000422716.1:n.688+57T>A
|
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ENST00000503121.5:c.242+1672T>A
|
|
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ENST00000505054.2:n.395-1108T>A
|
|
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NM_001039876.1:c.745T>A
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NP_001034965.1:p.Trp249Arg
|
|
NM_001039876.2:c.745T>A
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NP_001034965.1:p.Trp249Arg
|
|
NM_001297735.1:c.406T>A
|
NP_001284664.1:p.Trp136Arg
|
|
NM_001297735.2:c.406T>A
|
NP_001284664.1:p.Trp136Arg
|
|
XM_005258598.2:c.688+57T>A
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XP_005258655.1:n.688+57T>A
|
|
XM_005258601.2:c.618+205T>A
|
XP_005258658.1:n.618+205T>A
|
|
XM_005258604.3:c.688+57T>A
|
XP_005258661.1:n.688+57T>A
|
|
NM_001039876.3:c.745T>A
MANE Select
|
NP_001034965.1:p.Trp249Arg
|
|
NM_001297735.3:c.406T>A
|
NP_001284664.1:p.Trp136Arg
|
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