ENST00000269571.10:c.3622C>G
MANE Select
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ENSP00000269571.4:p.His1208Asp
|
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ENST00000269571.9:c.3622C>G
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ENSP00000269571.4:p.His1208Asp
|
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ENST00000406381.6:c.3532C>G
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ENSP00000385185.2:p.His1178Asp
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ENST00000445658.6:c.2794C>G
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ENSP00000404047.2:p.His932Asp
|
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ENST00000541774.5:c.3577C>G
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ENSP00000446466.1:p.His1193Asp
|
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ENST00000578373.5:c.*3412C>G
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ENSP00000463427.1:n.*3412C>G
|
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ENST00000584450.5:c.*201C>G
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ENSP00000463714.1:n.*201C>G
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ENST00000584601.5:c.3532C>G
|
ENSP00000462438.1:p.His1178Asp
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NM_001005862.2:c.3532C>G , LRG_724t1:c.3532C>G
|
NP_001005862.1:p.His1178Asp
|
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NM_001289936.1:c.3577C>G , LRG_724t4:c.3577C>G
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NP_001276865.1:p.His1193Asp
|
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NM_001289937.1:c.*201C>G
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NP_001276866.1:n.*201C>G
|
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NM_004448.3:c.3622C>G , LRG_724t2:c.3622C>G
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NP_004439.2:p.His1208Asp
|
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NR_110535.1:n.3946C>G
|
|
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XM_024450641.1:c.3760C>G
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XP_024306409.1:p.His1254Asp
|
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XM_024450642.1:c.3715C>G
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XP_024306410.1:p.His1239Asp
|
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XM_024450643.1:c.3670C>G
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XP_024306411.1:p.His1224Asp
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NM_001005862.3:c.3532C>G
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NP_001005862.1:p.His1178Asp
|
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NM_001289936.2:c.3577C>G
|
NP_001276865.1:p.His1193Asp
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NM_001289937.2:c.*201C>G
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NP_001276866.1:n.*201C>G
|
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NM_001382782.1:c.3532C>G
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NP_001369711.1:p.His1178Asp
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NM_001382783.1:c.3532C>G
|
NP_001369712.1:p.His1178Asp
|
|
NM_001382784.1:c.3739C>G
|
NP_001369713.1:p.His1247Asp
|
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NM_001382785.1:c.3724C>G
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NP_001369714.1:p.His1242Asp
|
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NM_001382786.1:c.3703C>G
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NP_001369715.1:p.His1235Asp
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NM_001382787.1:c.3697C>G
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NP_001369716.1:p.His1233Asp
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NM_001382788.1:c.3652C>G
|
NP_001369717.1:p.His1218Asp
|
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NM_001382789.1:c.3643C>G
|
NP_001369718.1:p.His1215Asp
|
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NM_001382790.1:c.3619C>G
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NP_001369719.1:p.His1207Asp
|
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NM_001382791.1:c.3613C>G
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NP_001369720.1:p.His1205Asp
|
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NM_001382792.1:c.3586C>G
|
NP_001369721.1:p.His1196Asp
|
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NM_001382793.1:c.3580C>G
|
NP_001369722.1:p.His1194Asp
|
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NM_001382794.1:c.3580C>G
|
NP_001369723.1:p.His1194Asp
|
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NM_001382795.1:c.3574C>G
|
NP_001369724.1:p.His1192Asp
|
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NM_001382796.1:c.3535C>G
|
NP_001369725.1:p.His1179Asp
|
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NM_001382797.1:c.3523C>G
|
NP_001369726.1:p.His1175Asp
|
|
NM_001382798.1:c.3466C>G
|
NP_001369727.1:p.His1156Asp
|
|
NM_001382799.1:c.3442C>G
|
NP_001369728.1:p.His1148Asp
|
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NM_001382800.1:c.3436C>G
|
NP_001369729.1:p.His1146Asp
|
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NM_001382801.1:c.3418C>G
|
NP_001369730.1:p.His1140Asp
|
|
NM_001382802.1:c.3364C>G
|
NP_001369731.1:p.His1122Asp
|
|
NM_001382803.1:c.*201C>G
|
NP_001369732.1:n.*201C>G
|
|
NM_001382804.1:c.2794C>G
|
NP_001369733.1:p.His932Asp
|
|
NM_001382805.1:c.2671C>G
|
NP_001369734.1:p.His891Asp
|
|
NM_001382806.1:c.2584C>G
|
NP_001369735.1:p.His862Asp
|
|
NM_004448.4:c.3622C>G
MANE Select
|
NP_004439.2:p.His1208Asp
|
|
NR_110535.2:n.3860C>G
|
|
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