ENST00000283871.10:c.878C>G
MANE Select
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ENSP00000283871.5:p.Ala293Gly
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ENST00000283871.9:c.878C>G
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ENSP00000283871.5:p.Ala293Gly
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ENST00000470321.1:n.218C>G
|
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ENST00000475447.2:c.306C>G
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ENST00000492108.5:c.284C>G
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ENSP00000419838.1:p.Ala95Gly
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ENST00000494453.1:c.298C>G
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NM_000187.3:c.878C>G
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NP_000178.2:p.Ala293Gly
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XM_005247412.1:c.653C>G
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XP_005247469.1:p.Ala218Gly
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XM_005247413.1:c.878C>G
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XP_005247470.1:p.Ala293Gly
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XM_011512746.1:c.878C>G
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XP_011511048.1:p.Ala293Gly
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XM_005247412.2:c.653C>G
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XP_005247469.1:p.Ala218Gly
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XM_005247413.2:c.878C>G
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XP_005247470.1:p.Ala293Gly
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XM_011512746.2:c.878C>G
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XP_011511048.1:p.Ala293Gly
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XM_017006277.2:c.455C>G
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XP_016861766.1:p.Ala152Gly
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NM_000187.4:c.878C>G
MANE Select
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NP_000178.2:p.Ala293Gly
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