ENST00000290866.10:c.3886C>G
MANE Select
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ENSP00000290866.4:p.Gln1296Glu
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ENST00000290863.10:c.2164C>G
|
ENSP00000290863.6:p.Gln722Glu
|
|
ENST00000290866.9:c.3886C>G
|
ENSP00000290866.4:p.Gln1296Glu
|
|
ENST00000413513.7:c.2041C>G
|
ENSP00000392247.3:p.Gln681Glu
|
|
ENST00000428043.5:c.*308C>G
|
ENSP00000397593.2:n.*308C>G
|
|
ENST00000577647.2:c.1969+346C>G
|
ENSP00000464149.1:n.1969+346C>G
|
|
ENST00000578839.5:c.*1641C>G
|
ENSP00000462110.2:n.*1641C>G
|
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ENST00000579314.5:c.*1615C>G
|
ENSP00000462599.1:n.*1615C>G
|
|
NM_000789.3:c.3886C>G
|
NP_000780.1:p.Gln1296Glu
|
|
NM_001178057.1:c.2041C>G
|
NP_001171528.1:p.Gln681Glu
|
|
NM_152830.2:c.2164C>G
|
NP_690043.1:p.Gln722Glu
|
|
XM_005257110.1:c.3337C>G
|
XP_005257167.1:p.Gln1113Glu
|
|
XM_006721737.2:c.2224C>G
|
XP_006721800.2:p.Gln742Glu
|
|
XM_006721737.3:c.2224C>G
|
XP_006721800.2:p.Gln742Glu
|
|
NM_000789.4:c.3886C>G
MANE Select
|
NP_000780.1:p.Gln1296Glu
|
|
NM_001178057.2:c.2041C>G
|
NP_001171528.1:p.Gln681Glu
|
|
NM_152830.3:c.2164C>G
|
NP_690043.1:p.Gln722Glu
|
|
NM_001382700.1:c.3319C>G
|
NP_001369629.1:p.Gln1107Glu
|
|
NM_001382701.1:c.3034C>G
|
NP_001369630.1:p.Gln1012Glu
|
|
NM_001382702.1:c.1501C>G
|
NP_001369631.1:p.Gln501Glu
|
|
NR_168483.1:n.2264C>G
|
|
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