ENST00000420175.3:c.434C>T
MANE Select
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ENSP00000391137.2:p.Ala145Val
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ENST00000275838.5:c.434C>T
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ENSP00000275838.1:p.Ala145Val
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ENST00000377867.7:c.389C>T
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ENSP00000367098.3:p.Ala130Val
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ENST00000420175.2:c.434C>T
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ENSP00000391137.2:p.Ala145Val
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NM_001142459.1:c.434C>T
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NP_001135931.2:p.Ala145Val
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NM_001142460.1:c.434C>T
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NP_001135932.2:p.Ala145Val
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NM_080871.3:c.389C>T
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NP_543147.2:p.Ala130Val
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XM_005249949.3:c.569C>T
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XP_005250006.1:p.Ala190Val
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NM_001142459.2:c.434C>T
MANE Select
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NP_001135931.2:p.Ala145Val
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NM_080871.4:c.389C>T
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NP_543147.2:p.Ala130Val
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