ENST00000269571.10:c.3420G>C
MANE Select
|
ENSP00000269571.4:p.Val1140=
|
|
ENST00000269571.9:c.3420G>C
|
ENSP00000269571.4:p.Val1140=
|
|
ENST00000406381.6:c.3330G>C
|
ENSP00000385185.2:p.Val1110=
|
|
ENST00000445658.6:c.2592G>C
|
ENSP00000404047.2:p.Val864=
|
|
ENST00000541774.5:c.3375G>C
|
ENSP00000446466.1:p.Val1125=
|
|
ENST00000578373.5:c.*3210G>C
|
ENSP00000463427.1:n.*3210G>C
|
|
ENST00000584450.5:c.3167G>C
|
ENSP00000463714.1:p.Ter1056Ser
|
|
ENST00000584601.5:c.3330G>C
|
ENSP00000462438.1:p.Val1110=
|
|
NM_001005862.2:c.3330G>C , LRG_724t1:c.3330G>C
|
NP_001005862.1:p.Val1110=
|
|
NM_001289936.1:c.3375G>C , LRG_724t4:c.3375G>C
|
NP_001276865.1:p.Val1125=
|
|
NM_001289937.1:c.3167G>C
|
NP_001276866.1:p.Ter1056Ser
|
|
NM_004448.3:c.3420G>C , LRG_724t2:c.3420G>C
|
NP_004439.2:p.Val1140=
|
|
NR_110535.1:n.3744G>C
|
|
|
XM_024450641.1:c.3558G>C
|
XP_024306409.1:p.Val1186=
|
|
XM_024450642.1:c.3513G>C
|
XP_024306410.1:p.Val1171=
|
|
XM_024450643.1:c.3468G>C
|
XP_024306411.1:p.Val1156=
|
|
NM_001005862.3:c.3330G>C
|
NP_001005862.1:p.Val1110=
|
|
NM_001289936.2:c.3375G>C
|
NP_001276865.1:p.Val1125=
|
|
NM_001289937.2:c.3167G>C
|
NP_001276866.1:p.Ter1056Ser
|
|
NM_001382782.1:c.3330G>C
|
NP_001369711.1:p.Val1110=
|
|
NM_001382783.1:c.3330G>C
|
NP_001369712.1:p.Val1110=
|
|
NM_001382784.1:c.3537G>C
|
NP_001369713.1:p.Val1179=
|
|
NM_001382785.1:c.3522G>C
|
NP_001369714.1:p.Val1174=
|
|
NM_001382786.1:c.3501G>C
|
NP_001369715.1:p.Val1167=
|
|
NM_001382787.1:c.3495G>C
|
NP_001369716.1:p.Val1165=
|
|
NM_001382788.1:c.3450G>C
|
NP_001369717.1:p.Val1150=
|
|
NM_001382789.1:c.3441G>C
|
NP_001369718.1:p.Val1147=
|
|
NM_001382790.1:c.3417G>C
|
NP_001369719.1:p.Val1139=
|
|
NM_001382791.1:c.3411G>C
|
NP_001369720.1:p.Val1137=
|
|
NM_001382792.1:c.3384G>C
|
NP_001369721.1:p.Val1128=
|
|
NM_001382793.1:c.3378G>C
|
NP_001369722.1:p.Val1126=
|
|
NM_001382794.1:c.3378G>C
|
NP_001369723.1:p.Val1126=
|
|
NM_001382795.1:c.3372G>C
|
NP_001369724.1:p.Val1124=
|
|
NM_001382796.1:c.3333G>C
|
NP_001369725.1:p.Val1111=
|
|
NM_001382797.1:c.3321G>C
|
NP_001369726.1:p.Val1107=
|
|
NM_001382798.1:c.3264G>C
|
NP_001369727.1:p.Val1088=
|
|
NM_001382799.1:c.3240G>C
|
NP_001369728.1:p.Val1080=
|
|
NM_001382800.1:c.3234G>C
|
NP_001369729.1:p.Val1078=
|
|
NM_001382801.1:c.3216G>C
|
NP_001369730.1:p.Val1072=
|
|
NM_001382802.1:c.3162G>C
|
NP_001369731.1:p.Val1054=
|
|
NM_001382803.1:c.3125G>C
|
NP_001369732.1:p.Ter1042Ser
|
|
NM_001382804.1:c.2592G>C
|
NP_001369733.1:p.Val864=
|
|
NM_001382805.1:c.2469G>C
|
NP_001369734.1:p.Val823=
|
|
NM_001382806.1:c.2382G>C
|
NP_001369735.1:p.Val794=
|
|
NM_004448.4:c.3420G>C
MANE Select
|
NP_004439.2:p.Val1140=
|
|
NR_110535.2:n.3658G>C
|
|
|