ENST00000290866.10:c.3510C>G
MANE Select
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ENSP00000290866.4:p.Ala1170=
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ENST00000290863.10:c.1788C>G
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ENSP00000290863.6:p.Ala596=
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ENST00000290866.9:c.3510C>G
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ENSP00000290866.4:p.Ala1170=
|
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ENST00000413513.7:c.1665C>G
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ENSP00000392247.3:p.Ala555=
|
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ENST00000428043.5:c.3510C>G
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ENSP00000397593.2:p.Ala1170=
|
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ENST00000577418.5:n.520C>G
|
|
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ENST00000577647.2:c.1788C>G
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ENSP00000464149.1:p.Ala596=
|
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ENST00000578839.5:c.*1265C>G
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ENSP00000462110.2:n.*1265C>G
|
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ENST00000579314.5:c.*1239C>G
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ENSP00000462599.1:n.*1239C>G
|
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ENST00000579409.1:c.197C>G
|
|
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ENST00000582244.1:n.384C>G
|
|
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NM_000789.3:c.3510C>G
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NP_000780.1:p.Ala1170=
|
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NM_001178057.1:c.1665C>G
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NP_001171528.1:p.Ala555=
|
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NM_152830.2:c.1788C>G
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NP_690043.1:p.Ala596=
|
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XM_005257110.1:c.2961C>G
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XP_005257167.1:p.Ala987=
|
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XM_006721737.2:c.1848C>G
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XP_006721800.2:p.Ala616=
|
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XM_006721737.3:c.1848C>G
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XP_006721800.2:p.Ala616=
|
|
NM_000789.4:c.3510C>G
MANE Select
|
NP_000780.1:p.Ala1170=
|
|
NM_001178057.2:c.1665C>G
|
NP_001171528.1:p.Ala555=
|
|
NM_152830.3:c.1788C>G
|
NP_690043.1:p.Ala596=
|
|
NM_001382700.1:c.2943C>G
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NP_001369629.1:p.Ala981=
|
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NM_001382701.1:c.2658C>G
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NP_001369630.1:p.Ala886=
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NM_001382702.1:c.1125C>G
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NP_001369631.1:p.Ala375=
|
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NR_168483.1:n.1888C>G
|
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