ENST00000378364.8:c.377T>C
MANE Select
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ENSP00000367615.3:p.Val126Ala
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ENST00000378364.7:c.377T>C
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ENSP00000367615.3:p.Val126Ala
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ENST00000426324.6:c.377T>C
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ENSP00000397007.2:p.Val126Ala
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ENST00000562464.1:n.387T>C
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ENST00000563655.5:c.296T>C
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ENSP00000456012.1:p.Val99Ala
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ENST00000567057.5:n.176T>C
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|
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ENST00000567391.5:c.*51T>C
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ENSP00000457964.1:n.*51T>C
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ENST00000567713.5:c.321+330T>C
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ENSP00000455749.1:n.321+330T>C
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ENST00000568319.5:c.*51T>C
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ENSP00000456905.1:n.*51T>C
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ENST00000568575.1:n.306T>C
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|
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ENST00000569616.1:c.375T>C
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|
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NM_000485.2:c.377T>C
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NP_000476.1:p.Val126Ala
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NM_001030018.1:c.377T>C
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NP_001025189.1:p.Val126Ala
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NM_000485.3:c.377T>C
MANE Select
|
NP_000476.1:p.Val126Ala
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NM_001030018.2:c.377T>C
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NP_001025189.1:p.Val126Ala
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