ENST00000322213.9:c.945C>G
MANE Select
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ENSP00000323421.3:p.Ala315=
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ENST00000674590.1:c.346-262C>G
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ENSP00000502626.1:n.346-262C>G
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ENST00000675065.1:n.466-262C>G
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|
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ENST00000675504.1:c.879C>G
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ENSP00000502524.1:p.Ala293=
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ENST00000322213.8:c.945C>G
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ENSP00000323421.3:p.Ala315=
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ENST00000375340.10:c.879C>G
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ENSP00000364489.7:p.Ala293=
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ENST00000463684.1:c.*478C>G
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ENSP00000476958.1:n.*478C>G
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NM_001281463.1:c.879C>G , LRG_773t1:c.879C>G
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NP_001268392.1:p.Ala293=
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NM_006306.3:c.945C>G , LRG_773t2:c.945C>G
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NP_006297.2:p.Ala315=
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NM_006306.4:c.945C>G
MANE Select
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NP_006297.2:p.Ala315=
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