ENST00000258385.8:c.1163A>C
MANE Select
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ENSP00000258385.3:p.Glu388Ala
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ENST00000258385.7:c.1163A>C
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ENSP00000258385.3:p.Glu388Ala
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ENST00000441621.6:c.*345A>C
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ENSP00000408819.2:n.*345A>C
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ENST00000446616.1:c.*804A>C
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ENSP00000410801.1:n.*804A>C
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ENST00000543200.5:c.1118A>C
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ENSP00000438380.1:p.Glu373Ala
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NM_000751.2:c.1163A>C
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NP_000742.1:p.Glu388Ala
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NM_001256657.1:c.1118A>C
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NP_001243586.1:p.Glu373Ala
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NM_001311195.1:c.581A>C
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NP_001298124.1:p.Glu194Ala
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NM_001311196.1:c.860A>C
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NP_001298125.1:p.Glu287Ala
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NR_046333.1:c.-4294966388A>C
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NR_046334.1:c.-4294966109A>C
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XM_011510524.1:c.782A>C
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XP_011508826.1:p.Glu261Ala
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XM_011510524.2:c.782A>C
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XP_011508826.1:p.Glu261Ala
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NM_000751.3:c.1163A>C
MANE Select
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NP_000742.1:p.Glu388Ala
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NM_001311195.2:c.581A>C
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NP_001298124.1:p.Glu194Ala
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NM_001311196.2:c.860A>C
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NP_001298125.1:p.Glu287Ala
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NM_001256657.2:c.1118A>C
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NP_001243586.1:p.Glu373Ala
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