ENST00000269571.10:c.3278G>T
MANE Select
|
ENSP00000269571.4:p.Gly1093Val
|
|
ENST00000269571.9:c.3278G>T
|
ENSP00000269571.4:p.Gly1093Val
|
|
ENST00000406381.6:c.3188G>T
|
ENSP00000385185.2:p.Gly1063Val
|
|
ENST00000445658.6:c.2450G>T
|
ENSP00000404047.2:p.Gly817Val
|
|
ENST00000541774.5:c.3233G>T
|
ENSP00000446466.1:p.Gly1078Val
|
|
ENST00000578373.5:c.*3068G>T
|
ENSP00000463427.1:n.*3068G>T
|
|
ENST00000584450.5:c.3160-276G>T
|
ENSP00000463714.1:n.3160-276G>T
|
|
ENST00000584601.5:c.3188G>T
|
ENSP00000462438.1:p.Gly1063Val
|
|
NM_001005862.2:c.3188G>T , LRG_724t1:c.3188G>T
|
NP_001005862.1:p.Gly1063Val
|
|
NM_001289936.1:c.3233G>T , LRG_724t4:c.3233G>T
|
NP_001276865.1:p.Gly1078Val
|
|
NM_001289937.1:c.3160-276G>T
|
NP_001276866.1:n.3160-276G>T
|
|
NM_004448.3:c.3278G>T , LRG_724t2:c.3278G>T
|
NP_004439.2:p.Gly1093Val
|
|
NR_110535.1:n.3602G>T
|
|
|
XM_024450641.1:c.3416G>T
|
XP_024306409.1:p.Gly1139Val
|
|
XM_024450642.1:c.3371G>T
|
XP_024306410.1:p.Gly1124Val
|
|
XM_024450643.1:c.3326G>T
|
XP_024306411.1:p.Gly1109Val
|
|
NM_001005862.3:c.3188G>T
|
NP_001005862.1:p.Gly1063Val
|
|
NM_001289936.2:c.3233G>T
|
NP_001276865.1:p.Gly1078Val
|
|
NM_001289937.2:c.3160-276G>T
|
NP_001276866.1:n.3160-276G>T
|
|
NM_001382782.1:c.3188G>T
|
NP_001369711.1:p.Gly1063Val
|
|
NM_001382783.1:c.3188G>T
|
NP_001369712.1:p.Gly1063Val
|
|
NM_001382784.1:c.3395G>T
|
NP_001369713.1:p.Gly1132Val
|
|
NM_001382785.1:c.3380G>T
|
NP_001369714.1:p.Gly1127Val
|
|
NM_001382786.1:c.3359G>T
|
NP_001369715.1:p.Gly1120Val
|
|
NM_001382787.1:c.3353G>T
|
NP_001369716.1:p.Gly1118Val
|
|
NM_001382788.1:c.3308G>T
|
NP_001369717.1:p.Gly1103Val
|
|
NM_001382789.1:c.3299G>T
|
NP_001369718.1:p.Gly1100Val
|
|
NM_001382790.1:c.3275G>T
|
NP_001369719.1:p.Gly1092Val
|
|
NM_001382791.1:c.3269G>T
|
NP_001369720.1:p.Gly1090Val
|
|
NM_001382792.1:c.3242G>T
|
NP_001369721.1:p.Gly1081Val
|
|
NM_001382793.1:c.3236G>T
|
NP_001369722.1:p.Gly1079Val
|
|
NM_001382794.1:c.3236G>T
|
NP_001369723.1:p.Gly1079Val
|
|
NM_001382795.1:c.3230G>T
|
NP_001369724.1:p.Gly1077Val
|
|
NM_001382796.1:c.3191G>T
|
NP_001369725.1:p.Gly1064Val
|
|
NM_001382797.1:c.3179G>T
|
NP_001369726.1:p.Gly1060Val
|
|
NM_001382798.1:c.3122G>T
|
NP_001369727.1:p.Gly1041Val
|
|
NM_001382799.1:c.3098G>T
|
NP_001369728.1:p.Gly1033Val
|
|
NM_001382800.1:c.3092G>T
|
NP_001369729.1:p.Gly1031Val
|
|
NM_001382801.1:c.3074G>T
|
NP_001369730.1:p.Gly1025Val
|
|
NM_001382802.1:c.3020G>T
|
NP_001369731.1:p.Gly1007Val
|
|
NM_001382803.1:c.3118-276G>T
|
NP_001369732.1:n.3118-276G>T
|
|
NM_001382804.1:c.2450G>T
|
NP_001369733.1:p.Gly817Val
|
|
NM_001382805.1:c.2327G>T
|
NP_001369734.1:p.Gly776Val
|
|
NM_001382806.1:c.2240G>T
|
NP_001369735.1:p.Gly747Val
|
|
NM_004448.4:c.3278G>T
MANE Select
|
NP_004439.2:p.Gly1093Val
|
|
NR_110535.2:n.3516G>T
|
|
|