ENST00000302804.12:c.686G>T
MANE Select
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ENSP00000302898.6:p.Cys229Phe
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ENST00000302804.11:c.686G>T
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ENSP00000302898.6:p.Cys229Phe
|
|
ENST00000415300.6:c.629G>T
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ENSP00000407162.1:p.Cys210Phe
|
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ENST00000448930.5:c.581G>T
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ENSP00000406798.2:p.Cys194Phe
|
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ENST00000594599.1:c.170G>T
|
ENSP00000469894.1:p.Cys57Phe
|
|
ENST00000596375.1:c.*247G>T
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ENSP00000470465.1:n.*247G>T
|
|
ENST00000598785.5:c.584G>T
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ENSP00000471830.1:p.Cys195Phe
|
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ENST00000599062.5:c.677G>T
|
ENSP00000469983.1:p.Cys226Phe
|
|
ENST00000601799.5:c.*985G>T
|
ENSP00000468918.1:n.*985G>T
|
|
NM_001015878.1:c.686G>T
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NP_001015878.1:p.Cys229Phe
|
|
NM_001015879.1:c.629G>T
|
NP_001015879.1:p.Cys210Phe
|
|
NM_003160.2:c.584G>T
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NP_003151.2:p.Cys195Phe
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XR_430209.2:n.1580G>T
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|
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XR_430209.3:n.1623G>T
|
|
|
NM_001015878.2:c.686G>T
MANE Select
|
NP_001015878.1:p.Cys229Phe
|
|
NM_001015879.2:c.629G>T
|
NP_001015879.1:p.Cys210Phe
|
|
NM_003160.3:c.584G>T
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NP_003151.2:p.Cys195Phe
|
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