ENST00000269571.10:c.3594A>T
MANE Select
|
ENSP00000269571.4:p.Thr1198=
|
|
ENST00000269571.9:c.3594A>T
|
ENSP00000269571.4:p.Thr1198=
|
|
ENST00000406381.6:c.3504A>T
|
ENSP00000385185.2:p.Thr1168=
|
|
ENST00000445658.6:c.2766A>T
|
ENSP00000404047.2:p.Thr922=
|
|
ENST00000541774.5:c.3549A>T
|
ENSP00000446466.1:p.Thr1183=
|
|
ENST00000578373.5:c.*3384A>T
|
ENSP00000463427.1:n.*3384A>T
|
|
ENST00000584450.5:c.*173A>T
|
ENSP00000463714.1:n.*173A>T
|
|
ENST00000584601.5:c.3504A>T
|
ENSP00000462438.1:p.Thr1168=
|
|
NM_001005862.2:c.3504A>T , LRG_724t1:c.3504A>T
|
NP_001005862.1:p.Thr1168=
|
|
NM_001289936.1:c.3549A>T , LRG_724t4:c.3549A>T
|
NP_001276865.1:p.Thr1183=
|
|
NM_001289937.1:c.*173A>T
|
NP_001276866.1:n.*173A>T
|
|
NM_004448.3:c.3594A>T , LRG_724t2:c.3594A>T
|
NP_004439.2:p.Thr1198=
|
|
NR_110535.1:n.3918A>T
|
|
|
XM_024450641.1:c.3732A>T
|
XP_024306409.1:p.Thr1244=
|
|
XM_024450642.1:c.3687A>T
|
XP_024306410.1:p.Thr1229=
|
|
XM_024450643.1:c.3642A>T
|
XP_024306411.1:p.Thr1214=
|
|
NM_001005862.3:c.3504A>T
|
NP_001005862.1:p.Thr1168=
|
|
NM_001289936.2:c.3549A>T
|
NP_001276865.1:p.Thr1183=
|
|
NM_001289937.2:c.*173A>T
|
NP_001276866.1:n.*173A>T
|
|
NM_001382782.1:c.3504A>T
|
NP_001369711.1:p.Thr1168=
|
|
NM_001382783.1:c.3504A>T
|
NP_001369712.1:p.Thr1168=
|
|
NM_001382784.1:c.3711A>T
|
NP_001369713.1:p.Thr1237=
|
|
NM_001382785.1:c.3696A>T
|
NP_001369714.1:p.Thr1232=
|
|
NM_001382786.1:c.3675A>T
|
NP_001369715.1:p.Thr1225=
|
|
NM_001382787.1:c.3669A>T
|
NP_001369716.1:p.Thr1223=
|
|
NM_001382788.1:c.3624A>T
|
NP_001369717.1:p.Thr1208=
|
|
NM_001382789.1:c.3615A>T
|
NP_001369718.1:p.Thr1205=
|
|
NM_001382790.1:c.3591A>T
|
NP_001369719.1:p.Thr1197=
|
|
NM_001382791.1:c.3585A>T
|
NP_001369720.1:p.Thr1195=
|
|
NM_001382792.1:c.3558A>T
|
NP_001369721.1:p.Thr1186=
|
|
NM_001382793.1:c.3552A>T
|
NP_001369722.1:p.Thr1184=
|
|
NM_001382794.1:c.3552A>T
|
NP_001369723.1:p.Thr1184=
|
|
NM_001382795.1:c.3546A>T
|
NP_001369724.1:p.Thr1182=
|
|
NM_001382796.1:c.3507A>T
|
NP_001369725.1:p.Thr1169=
|
|
NM_001382797.1:c.3495A>T
|
NP_001369726.1:p.Thr1165=
|
|
NM_001382798.1:c.3438A>T
|
NP_001369727.1:p.Thr1146=
|
|
NM_001382799.1:c.3414A>T
|
NP_001369728.1:p.Thr1138=
|
|
NM_001382800.1:c.3408A>T
|
NP_001369729.1:p.Thr1136=
|
|
NM_001382801.1:c.3390A>T
|
NP_001369730.1:p.Thr1130=
|
|
NM_001382802.1:c.3336A>T
|
NP_001369731.1:p.Thr1112=
|
|
NM_001382803.1:c.*173A>T
|
NP_001369732.1:n.*173A>T
|
|
NM_001382804.1:c.2766A>T
|
NP_001369733.1:p.Thr922=
|
|
NM_001382805.1:c.2643A>T
|
NP_001369734.1:p.Thr881=
|
|
NM_001382806.1:c.2556A>T
|
NP_001369735.1:p.Thr852=
|
|
NM_004448.4:c.3594A>T
MANE Select
|
NP_004439.2:p.Thr1198=
|
|
NR_110535.2:n.3832A>T
|
|
|