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ENST00000269571.10:c.3267C>G
MANE Select
|
ENSP00000269571.4:p.Asp1089Glu
|
|
|
ENST00000269571.9:c.3267C>G
|
ENSP00000269571.4:p.Asp1089Glu
|
|
|
ENST00000406381.6:c.3177C>G
|
ENSP00000385185.2:p.Asp1059Glu
|
|
|
ENST00000445658.6:c.2439C>G
|
ENSP00000404047.2:p.Asp813Glu
|
|
|
ENST00000541774.5:c.3222C>G
|
ENSP00000446466.1:p.Asp1074Glu
|
|
|
ENST00000578373.5:c.*3057C>G
|
ENSP00000463427.1:n.*3057C>G
|
|
|
ENST00000584450.5:c.3160-287C>G
|
ENSP00000463714.1:n.3160-287C>G
|
|
|
ENST00000584601.5:c.3177C>G
|
ENSP00000462438.1:p.Asp1059Glu
|
|
|
NM_001005862.2:c.3177C>G , LRG_724t1:c.3177C>G
|
NP_001005862.1:p.Asp1059Glu
|
|
|
NM_001289936.1:c.3222C>G , LRG_724t4:c.3222C>G
|
NP_001276865.1:p.Asp1074Glu
|
|
|
NM_001289937.1:c.3160-287C>G
|
NP_001276866.1:n.3160-287C>G
|
|
|
NM_004448.3:c.3267C>G , LRG_724t2:c.3267C>G
|
NP_004439.2:p.Asp1089Glu
|
|
|
NR_110535.1:n.3591C>G
|
|
|
|
XM_024450641.1:c.3405C>G
|
XP_024306409.1:p.Asp1135Glu
|
|
|
XM_024450642.1:c.3360C>G
|
XP_024306410.1:p.Asp1120Glu
|
|
|
XM_024450643.1:c.3315C>G
|
XP_024306411.1:p.Asp1105Glu
|
|
|
NM_001005862.3:c.3177C>G
|
NP_001005862.1:p.Asp1059Glu
|
|
|
NM_001289936.2:c.3222C>G
|
NP_001276865.1:p.Asp1074Glu
|
|
|
NM_001289937.2:c.3160-287C>G
|
NP_001276866.1:n.3160-287C>G
|
|
|
NM_001382782.1:c.3177C>G
|
NP_001369711.1:p.Asp1059Glu
|
|
|
NM_001382783.1:c.3177C>G
|
NP_001369712.1:p.Asp1059Glu
|
|
|
NM_001382784.1:c.3384C>G
|
NP_001369713.1:p.Asp1128Glu
|
|
|
NM_001382785.1:c.3369C>G
|
NP_001369714.1:p.Asp1123Glu
|
|
|
NM_001382786.1:c.3348C>G
|
NP_001369715.1:p.Asp1116Glu
|
|
|
NM_001382787.1:c.3342C>G
|
NP_001369716.1:p.Asp1114Glu
|
|
|
NM_001382788.1:c.3297C>G
|
NP_001369717.1:p.Asp1099Glu
|
|
|
NM_001382789.1:c.3288C>G
|
NP_001369718.1:p.Asp1096Glu
|
|
|
NM_001382790.1:c.3264C>G
|
NP_001369719.1:p.Asp1088Glu
|
|
|
NM_001382791.1:c.3258C>G
|
NP_001369720.1:p.Asp1086Glu
|
|
|
NM_001382792.1:c.3231C>G
|
NP_001369721.1:p.Asp1077Glu
|
|
|
NM_001382793.1:c.3225C>G
|
NP_001369722.1:p.Asp1075Glu
|
|
|
NM_001382794.1:c.3225C>G
|
NP_001369723.1:p.Asp1075Glu
|
|
|
NM_001382795.1:c.3219C>G
|
NP_001369724.1:p.Asp1073Glu
|
|
|
NM_001382796.1:c.3180C>G
|
NP_001369725.1:p.Asp1060Glu
|
|
|
NM_001382797.1:c.3168C>G
|
NP_001369726.1:p.Asp1056Glu
|
|
|
NM_001382798.1:c.3111C>G
|
NP_001369727.1:p.Asp1037Glu
|
|
|
NM_001382799.1:c.3087C>G
|
NP_001369728.1:p.Asp1029Glu
|
|
|
NM_001382800.1:c.3081C>G
|
NP_001369729.1:p.Asp1027Glu
|
|
|
NM_001382801.1:c.3063C>G
|
NP_001369730.1:p.Asp1021Glu
|
|
|
NM_001382802.1:c.3009C>G
|
NP_001369731.1:p.Asp1003Glu
|
|
|
NM_001382803.1:c.3118-287C>G
|
NP_001369732.1:n.3118-287C>G
|
|
|
NM_001382804.1:c.2439C>G
|
NP_001369733.1:p.Asp813Glu
|
|
|
NM_001382805.1:c.2316C>G
|
NP_001369734.1:p.Asp772Glu
|
|
|
NM_001382806.1:c.2229C>G
|
NP_001369735.1:p.Asp743Glu
|
|
|
NM_004448.4:c.3267C>G
MANE Select
|
NP_004439.2:p.Asp1089Glu
|
|
|
NR_110535.2:n.3505C>G
|
|
|
