ENST00000258385.8:c.1119C>G
MANE Select
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ENSP00000258385.3:p.Ala373=
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ENST00000258385.7:c.1119C>G
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ENSP00000258385.3:p.Ala373=
|
|
ENST00000441621.6:c.*301C>G
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ENSP00000408819.2:n.*301C>G
|
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ENST00000446616.1:c.*760C>G
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ENSP00000410801.1:n.*760C>G
|
|
ENST00000543200.5:c.1074C>G
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ENSP00000438380.1:p.Ala358=
|
|
NM_000751.2:c.1119C>G
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NP_000742.1:p.Ala373=
|
|
NM_001256657.1:c.1074C>G
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NP_001243586.1:p.Ala358=
|
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NM_001311195.1:c.537C>G
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NP_001298124.1:p.Ala179=
|
|
NM_001311196.1:c.816C>G
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NP_001298125.1:p.Ala272=
|
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NR_046333.1:c.-4294966432C>G
|
|
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NR_046334.1:c.-4294966153C>G
|
|
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XM_011510524.1:c.738C>G
|
XP_011508826.1:p.Ala246=
|
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XM_011510524.2:c.738C>G
|
XP_011508826.1:p.Ala246=
|
|
NM_000751.3:c.1119C>G
MANE Select
|
NP_000742.1:p.Ala373=
|
|
NM_001311195.2:c.537C>G
|
NP_001298124.1:p.Ala179=
|
|
NM_001311196.2:c.816C>G
|
NP_001298125.1:p.Ala272=
|
|
NM_001256657.2:c.1074C>G
|
NP_001243586.1:p.Ala358=
|
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