ENST00000597188.6:c.3269C>G
MANE Select
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ENSP00000471851.1:p.Ala1090Gly
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ENST00000270328.8:c.3269C>G
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ENSP00000270328.4:p.Ala1090Gly
|
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ENST00000593913.5:c.*2146C>G
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ENSP00000469901.1:n.*2146C>G
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ENST00000595838.5:c.1730C>G
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ENSP00000470501.1:p.Ala577Gly
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ENST00000597188.5:c.3269C>G
|
ENSP00000471851.1:p.Ala1090Gly
|
|
NM_001282352.1:c.1730C>G
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NP_001269281.1:p.Ala577Gly
|
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NM_030957.3:c.3269C>G
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NP_112219.3:p.Ala1090Gly
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XM_006722917.2:c.2312C>G
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XP_006722980.1:p.Ala771Gly
|
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XM_011528331.1:c.3416C>G
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XP_011526633.1:p.Ala1139Gly
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XM_011528332.1:c.3416C>G
|
XP_011526634.1:p.Ala1139Gly
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XM_011528333.1:c.3416C>G
|
XP_011526635.1:p.Ala1139Gly
|
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XM_011528334.1:c.3092C>G
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XP_011526636.1:p.Ala1031Gly
|
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XM_011528335.1:c.1985C>G
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XP_011526637.1:p.Ala662Gly
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XM_011528336.1:c.1979C>G
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XP_011526638.1:p.Ala660Gly
|
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XM_006722917.3:c.2312C>G
|
XP_006722980.1:p.Ala771Gly
|
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XM_017027338.2:c.3269C>G
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XP_016882827.1:p.Ala1090Gly
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XM_017027339.1:c.1838C>G
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XP_016882828.1:p.Ala613Gly
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XM_017027340.1:c.1832C>G
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XP_016882829.1:p.Ala611Gly
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NM_030957.4:c.3269C>G
MANE Select
|
NP_112219.3:p.Ala1090Gly
|
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NM_001282352.2:c.1730C>G
|
NP_001269281.1:p.Ala577Gly
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