ENST00000258385.8:c.1145G>T
MANE Select
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ENSP00000258385.3:p.Gly382Val
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ENST00000258385.7:c.1145G>T
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ENSP00000258385.3:p.Gly382Val
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ENST00000441621.6:c.*327G>T
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ENSP00000408819.2:n.*327G>T
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ENST00000446616.1:c.*786G>T
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ENSP00000410801.1:n.*786G>T
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ENST00000543200.5:c.1100G>T
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ENSP00000438380.1:p.Gly367Val
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NM_000751.2:c.1145G>T
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NP_000742.1:p.Gly382Val
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NM_001256657.1:c.1100G>T
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NP_001243586.1:p.Gly367Val
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NM_001311195.1:c.563G>T
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NP_001298124.1:p.Gly188Val
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NM_001311196.1:c.842G>T
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NP_001298125.1:p.Gly281Val
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NR_046333.1:c.-4294966406G>T
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NR_046334.1:c.-4294966127G>T
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XM_011510524.1:c.764G>T
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XP_011508826.1:p.Gly255Val
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XM_011510524.2:c.764G>T
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XP_011508826.1:p.Gly255Val
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NM_000751.3:c.1145G>T
MANE Select
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NP_000742.1:p.Gly382Val
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NM_001311195.2:c.563G>T
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NP_001298124.1:p.Gly188Val
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NM_001311196.2:c.842G>T
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NP_001298125.1:p.Gly281Val
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NM_001256657.2:c.1100G>T
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NP_001243586.1:p.Gly367Val
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