ENST00000290866.10:c.3755C>G
MANE Select
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ENSP00000290866.4:p.Ala1252Gly
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ENST00000290863.10:c.2033C>G
|
ENSP00000290863.6:p.Ala678Gly
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ENST00000290866.9:c.3755C>G
|
ENSP00000290866.4:p.Ala1252Gly
|
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ENST00000413513.7:c.1910C>G
|
ENSP00000392247.3:p.Ala637Gly
|
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ENST00000428043.5:c.*177C>G
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ENSP00000397593.2:n.*177C>G
|
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ENST00000577647.2:c.1969+215C>G
|
ENSP00000464149.1:n.1969+215C>G
|
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ENST00000578839.5:c.*1510C>G
|
ENSP00000462110.2:n.*1510C>G
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ENST00000579314.5:c.*1484C>G
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ENSP00000462599.1:n.*1484C>G
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NM_000789.3:c.3755C>G
|
NP_000780.1:p.Ala1252Gly
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NM_001178057.1:c.1910C>G
|
NP_001171528.1:p.Ala637Gly
|
|
NM_152830.2:c.2033C>G
|
NP_690043.1:p.Ala678Gly
|
|
XM_005257110.1:c.3206C>G
|
XP_005257167.1:p.Ala1069Gly
|
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XM_006721737.2:c.2093C>G
|
XP_006721800.2:p.Ala698Gly
|
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XM_006721737.3:c.2093C>G
|
XP_006721800.2:p.Ala698Gly
|
|
NM_000789.4:c.3755C>G
MANE Select
|
NP_000780.1:p.Ala1252Gly
|
|
NM_001178057.2:c.1910C>G
|
NP_001171528.1:p.Ala637Gly
|
|
NM_152830.3:c.2033C>G
|
NP_690043.1:p.Ala678Gly
|
|
NM_001382700.1:c.3188C>G
|
NP_001369629.1:p.Ala1063Gly
|
|
NM_001382701.1:c.2903C>G
|
NP_001369630.1:p.Ala968Gly
|
|
NM_001382702.1:c.1370C>G
|
NP_001369631.1:p.Ala457Gly
|
|
NR_168483.1:n.2133C>G
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