|
ENST00000269571.10:c.3233C>G
MANE Select
|
ENSP00000269571.4:p.Ser1078Cys
|
|
|
ENST00000269571.9:c.3233C>G
|
ENSP00000269571.4:p.Ser1078Cys
|
|
|
ENST00000406381.6:c.3143C>G
|
ENSP00000385185.2:p.Ser1048Cys
|
|
|
ENST00000445658.6:c.2405C>G
|
ENSP00000404047.2:p.Ser802Cys
|
|
|
ENST00000541774.5:c.3188C>G
|
ENSP00000446466.1:p.Ser1063Cys
|
|
|
ENST00000578373.5:c.*3023C>G
|
ENSP00000463427.1:n.*3023C>G
|
|
|
ENST00000584450.5:c.3160-321C>G
|
ENSP00000463714.1:n.3160-321C>G
|
|
|
ENST00000584601.5:c.3143C>G
|
ENSP00000462438.1:p.Ser1048Cys
|
|
|
NM_001005862.2:c.3143C>G , LRG_724t1:c.3143C>G
|
NP_001005862.1:p.Ser1048Cys
|
|
|
NM_001289936.1:c.3188C>G , LRG_724t4:c.3188C>G
|
NP_001276865.1:p.Ser1063Cys
|
|
|
NM_001289937.1:c.3160-321C>G
|
NP_001276866.1:n.3160-321C>G
|
|
|
NM_004448.3:c.3233C>G , LRG_724t2:c.3233C>G
|
NP_004439.2:p.Ser1078Cys
|
|
|
NR_110535.1:n.3557C>G
|
|
|
|
XM_024450641.1:c.3371C>G
|
XP_024306409.1:p.Ser1124Cys
|
|
|
XM_024450642.1:c.3326C>G
|
XP_024306410.1:p.Ser1109Cys
|
|
|
XM_024450643.1:c.3281C>G
|
XP_024306411.1:p.Ser1094Cys
|
|
|
NM_001005862.3:c.3143C>G
|
NP_001005862.1:p.Ser1048Cys
|
|
|
NM_001289936.2:c.3188C>G
|
NP_001276865.1:p.Ser1063Cys
|
|
|
NM_001289937.2:c.3160-321C>G
|
NP_001276866.1:n.3160-321C>G
|
|
|
NM_001382782.1:c.3143C>G
|
NP_001369711.1:p.Ser1048Cys
|
|
|
NM_001382783.1:c.3143C>G
|
NP_001369712.1:p.Ser1048Cys
|
|
|
NM_001382784.1:c.3350C>G
|
NP_001369713.1:p.Ser1117Cys
|
|
|
NM_001382785.1:c.3335C>G
|
NP_001369714.1:p.Ser1112Cys
|
|
|
NM_001382786.1:c.3314C>G
|
NP_001369715.1:p.Ser1105Cys
|
|
|
NM_001382787.1:c.3308C>G
|
NP_001369716.1:p.Ser1103Cys
|
|
|
NM_001382788.1:c.3263C>G
|
NP_001369717.1:p.Ser1088Cys
|
|
|
NM_001382789.1:c.3254C>G
|
NP_001369718.1:p.Ser1085Cys
|
|
|
NM_001382790.1:c.3230C>G
|
NP_001369719.1:p.Ser1077Cys
|
|
|
NM_001382791.1:c.3224C>G
|
NP_001369720.1:p.Ser1075Cys
|
|
|
NM_001382792.1:c.3197C>G
|
NP_001369721.1:p.Ser1066Cys
|
|
|
NM_001382793.1:c.3191C>G
|
NP_001369722.1:p.Ser1064Cys
|
|
|
NM_001382794.1:c.3191C>G
|
NP_001369723.1:p.Ser1064Cys
|
|
|
NM_001382795.1:c.3185C>G
|
NP_001369724.1:p.Ser1062Cys
|
|
|
NM_001382796.1:c.3146C>G
|
NP_001369725.1:p.Ser1049Cys
|
|
|
NM_001382797.1:c.3134C>G
|
NP_001369726.1:p.Ser1045Cys
|
|
|
NM_001382798.1:c.3077C>G
|
NP_001369727.1:p.Ser1026Cys
|
|
|
NM_001382799.1:c.3053C>G
|
NP_001369728.1:p.Ser1018Cys
|
|
|
NM_001382800.1:c.3047C>G
|
NP_001369729.1:p.Ser1016Cys
|
|
|
NM_001382801.1:c.3029C>G
|
NP_001369730.1:p.Ser1010Cys
|
|
|
NM_001382802.1:c.2975C>G
|
NP_001369731.1:p.Ser992Cys
|
|
|
NM_001382803.1:c.3118-321C>G
|
NP_001369732.1:n.3118-321C>G
|
|
|
NM_001382804.1:c.2405C>G
|
NP_001369733.1:p.Ser802Cys
|
|
|
NM_001382805.1:c.2282C>G
|
NP_001369734.1:p.Ser761Cys
|
|
|
NM_001382806.1:c.2195C>G
|
NP_001369735.1:p.Ser732Cys
|
|
|
NM_004448.4:c.3233C>G
MANE Select
|
NP_004439.2:p.Ser1078Cys
|
|
|
NR_110535.2:n.3471C>G
|
|
|
