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ENST00000269571.10:c.3636C>G
MANE Select
|
ENSP00000269571.4:p.Ala1212=
|
|
|
ENST00000269571.9:c.3636C>G
|
ENSP00000269571.4:p.Ala1212=
|
|
|
ENST00000406381.6:c.3546C>G
|
ENSP00000385185.2:p.Ala1182=
|
|
|
ENST00000445658.6:c.2808C>G
|
ENSP00000404047.2:p.Ala936=
|
|
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ENST00000541774.5:c.3591C>G
|
ENSP00000446466.1:p.Ala1197=
|
|
|
ENST00000578373.5:c.*3426C>G
|
ENSP00000463427.1:n.*3426C>G
|
|
|
ENST00000584450.5:c.*215C>G
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ENSP00000463714.1:n.*215C>G
|
|
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ENST00000584601.5:c.3546C>G
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ENSP00000462438.1:p.Ala1182=
|
|
|
NM_001005862.2:c.3546C>G , LRG_724t1:c.3546C>G
|
NP_001005862.1:p.Ala1182=
|
|
|
NM_001289936.1:c.3591C>G , LRG_724t4:c.3591C>G
|
NP_001276865.1:p.Ala1197=
|
|
|
NM_001289937.1:c.*215C>G
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NP_001276866.1:n.*215C>G
|
|
|
NM_004448.3:c.3636C>G , LRG_724t2:c.3636C>G
|
NP_004439.2:p.Ala1212=
|
|
|
NR_110535.1:n.3960C>G
|
|
|
|
XM_024450641.1:c.3774C>G
|
XP_024306409.1:p.Ala1258=
|
|
|
XM_024450642.1:c.3729C>G
|
XP_024306410.1:p.Ala1243=
|
|
|
XM_024450643.1:c.3684C>G
|
XP_024306411.1:p.Ala1228=
|
|
|
NM_001005862.3:c.3546C>G
|
NP_001005862.1:p.Ala1182=
|
|
|
NM_001289936.2:c.3591C>G
|
NP_001276865.1:p.Ala1197=
|
|
|
NM_001289937.2:c.*215C>G
|
NP_001276866.1:n.*215C>G
|
|
|
NM_001382782.1:c.3546C>G
|
NP_001369711.1:p.Ala1182=
|
|
|
NM_001382783.1:c.3546C>G
|
NP_001369712.1:p.Ala1182=
|
|
|
NM_001382784.1:c.3753C>G
|
NP_001369713.1:p.Ala1251=
|
|
|
NM_001382785.1:c.3738C>G
|
NP_001369714.1:p.Ala1246=
|
|
|
NM_001382786.1:c.3717C>G
|
NP_001369715.1:p.Ala1239=
|
|
|
NM_001382787.1:c.3711C>G
|
NP_001369716.1:p.Ala1237=
|
|
|
NM_001382788.1:c.3666C>G
|
NP_001369717.1:p.Ala1222=
|
|
|
NM_001382789.1:c.3657C>G
|
NP_001369718.1:p.Ala1219=
|
|
|
NM_001382790.1:c.3633C>G
|
NP_001369719.1:p.Ala1211=
|
|
|
NM_001382791.1:c.3627C>G
|
NP_001369720.1:p.Ala1209=
|
|
|
NM_001382792.1:c.3600C>G
|
NP_001369721.1:p.Ala1200=
|
|
|
NM_001382793.1:c.3594C>G
|
NP_001369722.1:p.Ala1198=
|
|
|
NM_001382794.1:c.3594C>G
|
NP_001369723.1:p.Ala1198=
|
|
|
NM_001382795.1:c.3588C>G
|
NP_001369724.1:p.Ala1196=
|
|
|
NM_001382796.1:c.3549C>G
|
NP_001369725.1:p.Ala1183=
|
|
|
NM_001382797.1:c.3537C>G
|
NP_001369726.1:p.Ala1179=
|
|
|
NM_001382798.1:c.3480C>G
|
NP_001369727.1:p.Ala1160=
|
|
|
NM_001382799.1:c.3456C>G
|
NP_001369728.1:p.Ala1152=
|
|
|
NM_001382800.1:c.3450C>G
|
NP_001369729.1:p.Ala1150=
|
|
|
NM_001382801.1:c.3432C>G
|
NP_001369730.1:p.Ala1144=
|
|
|
NM_001382802.1:c.3378C>G
|
NP_001369731.1:p.Ala1126=
|
|
|
NM_001382803.1:c.*215C>G
|
NP_001369732.1:n.*215C>G
|
|
|
NM_001382804.1:c.2808C>G
|
NP_001369733.1:p.Ala936=
|
|
|
NM_001382805.1:c.2685C>G
|
NP_001369734.1:p.Ala895=
|
|
|
NM_001382806.1:c.2598C>G
|
NP_001369735.1:p.Ala866=
|
|
|
NM_004448.4:c.3636C>G
MANE Select
|
NP_004439.2:p.Ala1212=
|
|
|
NR_110535.2:n.3874C>G
|
|
|
