ENST00000258385.8:c.1166A>C
MANE Select
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ENSP00000258385.3:p.Glu389Ala
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ENST00000258385.7:c.1166A>C
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ENSP00000258385.3:p.Glu389Ala
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ENST00000441621.6:c.*348A>C
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ENSP00000408819.2:n.*348A>C
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ENST00000446616.1:c.*807A>C
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ENSP00000410801.1:n.*807A>C
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ENST00000543200.5:c.1121A>C
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ENSP00000438380.1:p.Glu374Ala
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NM_000751.2:c.1166A>C
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NP_000742.1:p.Glu389Ala
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NM_001256657.1:c.1121A>C
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NP_001243586.1:p.Glu374Ala
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NM_001311195.1:c.584A>C
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NP_001298124.1:p.Glu195Ala
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NM_001311196.1:c.863A>C
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NP_001298125.1:p.Glu288Ala
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NR_046333.1:c.-4294966385A>C
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NR_046334.1:c.-4294966106A>C
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XM_011510524.1:c.785A>C
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XP_011508826.1:p.Glu262Ala
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XM_011510524.2:c.785A>C
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XP_011508826.1:p.Glu262Ala
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NM_000751.3:c.1166A>C
MANE Select
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NP_000742.1:p.Glu389Ala
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NM_001311195.2:c.584A>C
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NP_001298124.1:p.Glu195Ala
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NM_001311196.2:c.863A>C
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NP_001298125.1:p.Glu288Ala
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NM_001256657.2:c.1121A>C
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NP_001243586.1:p.Glu374Ala
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