ENST00000269571.10:c.3609T>C
MANE Select
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ENSP00000269571.4:p.Ala1203=
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ENST00000269571.9:c.3609T>C
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ENSP00000269571.4:p.Ala1203=
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ENST00000406381.6:c.3519T>C
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ENSP00000385185.2:p.Ala1173=
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ENST00000445658.6:c.2781T>C
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ENSP00000404047.2:p.Ala927=
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ENST00000541774.5:c.3564T>C
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ENSP00000446466.1:p.Ala1188=
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ENST00000578373.5:c.*3399T>C
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ENSP00000463427.1:n.*3399T>C
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ENST00000584450.5:c.*188T>C
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ENSP00000463714.1:n.*188T>C
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ENST00000584601.5:c.3519T>C
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ENSP00000462438.1:p.Ala1173=
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NM_001005862.2:c.3519T>C , LRG_724t1:c.3519T>C
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NP_001005862.1:p.Ala1173=
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NM_001289936.1:c.3564T>C , LRG_724t4:c.3564T>C
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NP_001276865.1:p.Ala1188=
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NM_001289937.1:c.*188T>C
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NP_001276866.1:n.*188T>C
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NM_004448.3:c.3609T>C , LRG_724t2:c.3609T>C
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NP_004439.2:p.Ala1203=
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NR_110535.1:n.3933T>C
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XM_024450641.1:c.3747T>C
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XP_024306409.1:p.Ala1249=
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XM_024450642.1:c.3702T>C
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XP_024306410.1:p.Ala1234=
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XM_024450643.1:c.3657T>C
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XP_024306411.1:p.Ala1219=
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NM_001005862.3:c.3519T>C
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NP_001005862.1:p.Ala1173=
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NM_001289936.2:c.3564T>C
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NP_001276865.1:p.Ala1188=
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NM_001289937.2:c.*188T>C
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NP_001276866.1:n.*188T>C
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NM_001382782.1:c.3519T>C
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NP_001369711.1:p.Ala1173=
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NM_001382783.1:c.3519T>C
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NP_001369712.1:p.Ala1173=
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NM_001382784.1:c.3726T>C
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NP_001369713.1:p.Ala1242=
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NM_001382785.1:c.3711T>C
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NP_001369714.1:p.Ala1237=
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NM_001382786.1:c.3690T>C
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NP_001369715.1:p.Ala1230=
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NM_001382787.1:c.3684T>C
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NP_001369716.1:p.Ala1228=
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NM_001382788.1:c.3639T>C
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NP_001369717.1:p.Ala1213=
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NM_001382789.1:c.3630T>C
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NP_001369718.1:p.Ala1210=
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NM_001382790.1:c.3606T>C
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NP_001369719.1:p.Ala1202=
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NM_001382791.1:c.3600T>C
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NP_001369720.1:p.Ala1200=
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NM_001382792.1:c.3573T>C
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NP_001369721.1:p.Ala1191=
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NM_001382793.1:c.3567T>C
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NP_001369722.1:p.Ala1189=
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NM_001382794.1:c.3567T>C
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NP_001369723.1:p.Ala1189=
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NM_001382795.1:c.3561T>C
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NP_001369724.1:p.Ala1187=
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NM_001382796.1:c.3522T>C
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NP_001369725.1:p.Ala1174=
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NM_001382797.1:c.3510T>C
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NP_001369726.1:p.Ala1170=
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NM_001382798.1:c.3453T>C
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NP_001369727.1:p.Ala1151=
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NM_001382799.1:c.3429T>C
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NP_001369728.1:p.Ala1143=
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NM_001382800.1:c.3423T>C
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NP_001369729.1:p.Ala1141=
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NM_001382801.1:c.3405T>C
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NP_001369730.1:p.Ala1135=
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NM_001382802.1:c.3351T>C
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NP_001369731.1:p.Ala1117=
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NM_001382803.1:c.*188T>C
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NP_001369732.1:n.*188T>C
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NM_001382804.1:c.2781T>C
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NP_001369733.1:p.Ala927=
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NM_001382805.1:c.2658T>C
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NP_001369734.1:p.Ala886=
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NM_001382806.1:c.2571T>C
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NP_001369735.1:p.Ala857=
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NM_004448.4:c.3609T>C
MANE Select
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NP_004439.2:p.Ala1203=
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NR_110535.2:n.3847T>C
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