ENST00000359842.10:c.416G>T
MANE Select
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ENSP00000352900.5:p.Cys139Phe
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ENST00000359842.9:c.416G>T
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ENSP00000352900.5:p.Cys139Phe
|
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ENST00000470566.1:n.341G>T
|
|
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ENST00000619224.1:c.47G>T
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ENSP00000482458.1:p.Cys16Phe
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NM_001256570.1:c.47G>T
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NP_001243499.1:p.Cys16Phe
|
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NM_001256571.1:c.47G>T
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NP_001243500.1:p.Cys16Phe
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NM_006917.4:c.416G>T
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NP_008848.1:p.Cys139Phe
|
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NM_006917.5:c.416G>T
MANE Select
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NP_008848.1:p.Cys139Phe
|
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NM_001256571.2:c.47G>T
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NP_001243500.1:p.Cys16Phe
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NM_001256570.2:c.47G>T
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NP_001243499.1:p.Cys16Phe
|
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