ENST00000258385.8:c.1233C>G
MANE Select
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ENSP00000258385.3:p.Ala411=
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ENST00000258385.7:c.1233C>G
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ENSP00000258385.3:p.Ala411=
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ENST00000441621.6:c.*415C>G
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ENSP00000408819.2:n.*415C>G
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ENST00000446616.1:c.*874C>G
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ENSP00000410801.1:n.*874C>G
|
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ENST00000543200.5:c.1188C>G
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ENSP00000438380.1:p.Ala396=
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NM_000751.2:c.1233C>G
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NP_000742.1:p.Ala411=
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NM_001256657.1:c.1188C>G
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NP_001243586.1:p.Ala396=
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NM_001311195.1:c.651C>G
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NP_001298124.1:p.Ala217=
|
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NM_001311196.1:c.930C>G
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NP_001298125.1:p.Ala310=
|
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NR_046333.1:c.-4294966318C>G
|
|
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NR_046334.1:c.-4294966039C>G
|
|
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XM_011510524.1:c.852C>G
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XP_011508826.1:p.Ala284=
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XM_011510524.2:c.852C>G
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XP_011508826.1:p.Ala284=
|
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NM_000751.3:c.1233C>G
MANE Select
|
NP_000742.1:p.Ala411=
|
|
NM_001311195.2:c.651C>G
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NP_001298124.1:p.Ala217=
|
|
NM_001311196.2:c.930C>G
|
NP_001298125.1:p.Ala310=
|
|
NM_001256657.2:c.1188C>G
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NP_001243586.1:p.Ala396=
|
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