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ENST00000269571.10:c.3375T>G
MANE Select
|
ENSP00000269571.4:p.Asp1125Glu
|
|
|
ENST00000269571.9:c.3375T>G
|
ENSP00000269571.4:p.Asp1125Glu
|
|
|
ENST00000406381.6:c.3285T>G
|
ENSP00000385185.2:p.Asp1095Glu
|
|
|
ENST00000445658.6:c.2547T>G
|
ENSP00000404047.2:p.Asp849Glu
|
|
|
ENST00000541774.5:c.3330T>G
|
ENSP00000446466.1:p.Asp1110Glu
|
|
|
ENST00000578373.5:c.*3165T>G
|
ENSP00000463427.1:n.*3165T>G
|
|
|
ENST00000584450.5:c.3160-179T>G
|
ENSP00000463714.1:n.3160-179T>G
|
|
|
ENST00000584601.5:c.3285T>G
|
ENSP00000462438.1:p.Asp1095Glu
|
|
|
NM_001005862.2:c.3285T>G , LRG_724t1:c.3285T>G
|
NP_001005862.1:p.Asp1095Glu
|
|
|
NM_001289936.1:c.3330T>G , LRG_724t4:c.3330T>G
|
NP_001276865.1:p.Asp1110Glu
|
|
|
NM_001289937.1:c.3160-179T>G
|
NP_001276866.1:n.3160-179T>G
|
|
|
NM_004448.3:c.3375T>G , LRG_724t2:c.3375T>G
|
NP_004439.2:p.Asp1125Glu
|
|
|
NR_110535.1:n.3699T>G
|
|
|
|
XM_024450641.1:c.3513T>G
|
XP_024306409.1:p.Asp1171Glu
|
|
|
XM_024450642.1:c.3468T>G
|
XP_024306410.1:p.Asp1156Glu
|
|
|
XM_024450643.1:c.3423T>G
|
XP_024306411.1:p.Asp1141Glu
|
|
|
NM_001005862.3:c.3285T>G
|
NP_001005862.1:p.Asp1095Glu
|
|
|
NM_001289936.2:c.3330T>G
|
NP_001276865.1:p.Asp1110Glu
|
|
|
NM_001289937.2:c.3160-179T>G
|
NP_001276866.1:n.3160-179T>G
|
|
|
NM_001382782.1:c.3285T>G
|
NP_001369711.1:p.Asp1095Glu
|
|
|
NM_001382783.1:c.3285T>G
|
NP_001369712.1:p.Asp1095Glu
|
|
|
NM_001382784.1:c.3492T>G
|
NP_001369713.1:p.Asp1164Glu
|
|
|
NM_001382785.1:c.3477T>G
|
NP_001369714.1:p.Asp1159Glu
|
|
|
NM_001382786.1:c.3456T>G
|
NP_001369715.1:p.Asp1152Glu
|
|
|
NM_001382787.1:c.3450T>G
|
NP_001369716.1:p.Asp1150Glu
|
|
|
NM_001382788.1:c.3405T>G
|
NP_001369717.1:p.Asp1135Glu
|
|
|
NM_001382789.1:c.3396T>G
|
NP_001369718.1:p.Asp1132Glu
|
|
|
NM_001382790.1:c.3372T>G
|
NP_001369719.1:p.Asp1124Glu
|
|
|
NM_001382791.1:c.3366T>G
|
NP_001369720.1:p.Asp1122Glu
|
|
|
NM_001382792.1:c.3339T>G
|
NP_001369721.1:p.Asp1113Glu
|
|
|
NM_001382793.1:c.3333T>G
|
NP_001369722.1:p.Asp1111Glu
|
|
|
NM_001382794.1:c.3333T>G
|
NP_001369723.1:p.Asp1111Glu
|
|
|
NM_001382795.1:c.3327T>G
|
NP_001369724.1:p.Asp1109Glu
|
|
|
NM_001382796.1:c.3288T>G
|
NP_001369725.1:p.Asp1096Glu
|
|
|
NM_001382797.1:c.3276T>G
|
NP_001369726.1:p.Asp1092Glu
|
|
|
NM_001382798.1:c.3219T>G
|
NP_001369727.1:p.Asp1073Glu
|
|
|
NM_001382799.1:c.3195T>G
|
NP_001369728.1:p.Asp1065Glu
|
|
|
NM_001382800.1:c.3189T>G
|
NP_001369729.1:p.Asp1063Glu
|
|
|
NM_001382801.1:c.3171T>G
|
NP_001369730.1:p.Asp1057Glu
|
|
|
NM_001382802.1:c.3117T>G
|
NP_001369731.1:p.Asp1039Glu
|
|
|
NM_001382803.1:c.3118-179T>G
|
NP_001369732.1:n.3118-179T>G
|
|
|
NM_001382804.1:c.2547T>G
|
NP_001369733.1:p.Asp849Glu
|
|
|
NM_001382805.1:c.2424T>G
|
NP_001369734.1:p.Asp808Glu
|
|
|
NM_001382806.1:c.2337T>G
|
NP_001369735.1:p.Asp779Glu
|
|
|
NM_004448.4:c.3375T>G
MANE Select
|
NP_004439.2:p.Asp1125Glu
|
|
|
NR_110535.2:n.3613T>G
|
|
|
