|
ENST00000269571.10:c.3603A>G
MANE Select
|
ENSP00000269571.4:p.Gly1201=
|
|
|
ENST00000269571.9:c.3603A>G
|
ENSP00000269571.4:p.Gly1201=
|
|
|
ENST00000406381.6:c.3513A>G
|
ENSP00000385185.2:p.Gly1171=
|
|
|
ENST00000445658.6:c.2775A>G
|
ENSP00000404047.2:p.Gly925=
|
|
|
ENST00000541774.5:c.3558A>G
|
ENSP00000446466.1:p.Gly1186=
|
|
|
ENST00000578373.5:c.*3393A>G
|
ENSP00000463427.1:n.*3393A>G
|
|
|
ENST00000584450.5:c.*182A>G
|
ENSP00000463714.1:n.*182A>G
|
|
|
ENST00000584601.5:c.3513A>G
|
ENSP00000462438.1:p.Gly1171=
|
|
|
NM_001005862.2:c.3513A>G , LRG_724t1:c.3513A>G
|
NP_001005862.1:p.Gly1171=
|
|
|
NM_001289936.1:c.3558A>G , LRG_724t4:c.3558A>G
|
NP_001276865.1:p.Gly1186=
|
|
|
NM_001289937.1:c.*182A>G
|
NP_001276866.1:n.*182A>G
|
|
|
NM_004448.3:c.3603A>G , LRG_724t2:c.3603A>G
|
NP_004439.2:p.Gly1201=
|
|
|
NR_110535.1:n.3927A>G
|
|
|
|
XM_024450641.1:c.3741A>G
|
XP_024306409.1:p.Gly1247=
|
|
|
XM_024450642.1:c.3696A>G
|
XP_024306410.1:p.Gly1232=
|
|
|
XM_024450643.1:c.3651A>G
|
XP_024306411.1:p.Gly1217=
|
|
|
NM_001005862.3:c.3513A>G
|
NP_001005862.1:p.Gly1171=
|
|
|
NM_001289936.2:c.3558A>G
|
NP_001276865.1:p.Gly1186=
|
|
|
NM_001289937.2:c.*182A>G
|
NP_001276866.1:n.*182A>G
|
|
|
NM_001382782.1:c.3513A>G
|
NP_001369711.1:p.Gly1171=
|
|
|
NM_001382783.1:c.3513A>G
|
NP_001369712.1:p.Gly1171=
|
|
|
NM_001382784.1:c.3720A>G
|
NP_001369713.1:p.Gly1240=
|
|
|
NM_001382785.1:c.3705A>G
|
NP_001369714.1:p.Gly1235=
|
|
|
NM_001382786.1:c.3684A>G
|
NP_001369715.1:p.Gly1228=
|
|
|
NM_001382787.1:c.3678A>G
|
NP_001369716.1:p.Gly1226=
|
|
|
NM_001382788.1:c.3633A>G
|
NP_001369717.1:p.Gly1211=
|
|
|
NM_001382789.1:c.3624A>G
|
NP_001369718.1:p.Gly1208=
|
|
|
NM_001382790.1:c.3600A>G
|
NP_001369719.1:p.Gly1200=
|
|
|
NM_001382791.1:c.3594A>G
|
NP_001369720.1:p.Gly1198=
|
|
|
NM_001382792.1:c.3567A>G
|
NP_001369721.1:p.Gly1189=
|
|
|
NM_001382793.1:c.3561A>G
|
NP_001369722.1:p.Gly1187=
|
|
|
NM_001382794.1:c.3561A>G
|
NP_001369723.1:p.Gly1187=
|
|
|
NM_001382795.1:c.3555A>G
|
NP_001369724.1:p.Gly1185=
|
|
|
NM_001382796.1:c.3516A>G
|
NP_001369725.1:p.Gly1172=
|
|
|
NM_001382797.1:c.3504A>G
|
NP_001369726.1:p.Gly1168=
|
|
|
NM_001382798.1:c.3447A>G
|
NP_001369727.1:p.Gly1149=
|
|
|
NM_001382799.1:c.3423A>G
|
NP_001369728.1:p.Gly1141=
|
|
|
NM_001382800.1:c.3417A>G
|
NP_001369729.1:p.Gly1139=
|
|
|
NM_001382801.1:c.3399A>G
|
NP_001369730.1:p.Gly1133=
|
|
|
NM_001382802.1:c.3345A>G
|
NP_001369731.1:p.Gly1115=
|
|
|
NM_001382803.1:c.*182A>G
|
NP_001369732.1:n.*182A>G
|
|
|
NM_001382804.1:c.2775A>G
|
NP_001369733.1:p.Gly925=
|
|
|
NM_001382805.1:c.2652A>G
|
NP_001369734.1:p.Gly884=
|
|
|
NM_001382806.1:c.2565A>G
|
NP_001369735.1:p.Gly855=
|
|
|
NM_004448.4:c.3603A>G
MANE Select
|
NP_004439.2:p.Gly1201=
|
|
|
NR_110535.2:n.3841A>G
|
|
|
