|
ENST00000269571.10:c.3331C>G
MANE Select
|
ENSP00000269571.4:p.Arg1111Gly
|
|
|
ENST00000269571.9:c.3331C>G
|
ENSP00000269571.4:p.Arg1111Gly
|
|
|
ENST00000406381.6:c.3241C>G
|
ENSP00000385185.2:p.Arg1081Gly
|
|
|
ENST00000445658.6:c.2503C>G
|
ENSP00000404047.2:p.Arg835Gly
|
|
|
ENST00000541774.5:c.3286C>G
|
ENSP00000446466.1:p.Arg1096Gly
|
|
|
ENST00000578373.5:c.*3121C>G
|
ENSP00000463427.1:n.*3121C>G
|
|
|
ENST00000584450.5:c.3160-223C>G
|
ENSP00000463714.1:n.3160-223C>G
|
|
|
ENST00000584601.5:c.3241C>G
|
ENSP00000462438.1:p.Arg1081Gly
|
|
|
NM_001005862.2:c.3241C>G , LRG_724t1:c.3241C>G
|
NP_001005862.1:p.Arg1081Gly
|
|
|
NM_001289936.1:c.3286C>G , LRG_724t4:c.3286C>G
|
NP_001276865.1:p.Arg1096Gly
|
|
|
NM_001289937.1:c.3160-223C>G
|
NP_001276866.1:n.3160-223C>G
|
|
|
NM_004448.3:c.3331C>G , LRG_724t2:c.3331C>G
|
NP_004439.2:p.Arg1111Gly
|
|
|
NR_110535.1:n.3655C>G
|
|
|
|
XM_024450641.1:c.3469C>G
|
XP_024306409.1:p.Arg1157Gly
|
|
|
XM_024450642.1:c.3424C>G
|
XP_024306410.1:p.Arg1142Gly
|
|
|
XM_024450643.1:c.3379C>G
|
XP_024306411.1:p.Arg1127Gly
|
|
|
NM_001005862.3:c.3241C>G
|
NP_001005862.1:p.Arg1081Gly
|
|
|
NM_001289936.2:c.3286C>G
|
NP_001276865.1:p.Arg1096Gly
|
|
|
NM_001289937.2:c.3160-223C>G
|
NP_001276866.1:n.3160-223C>G
|
|
|
NM_001382782.1:c.3241C>G
|
NP_001369711.1:p.Arg1081Gly
|
|
|
NM_001382783.1:c.3241C>G
|
NP_001369712.1:p.Arg1081Gly
|
|
|
NM_001382784.1:c.3448C>G
|
NP_001369713.1:p.Arg1150Gly
|
|
|
NM_001382785.1:c.3433C>G
|
NP_001369714.1:p.Arg1145Gly
|
|
|
NM_001382786.1:c.3412C>G
|
NP_001369715.1:p.Arg1138Gly
|
|
|
NM_001382787.1:c.3406C>G
|
NP_001369716.1:p.Arg1136Gly
|
|
|
NM_001382788.1:c.3361C>G
|
NP_001369717.1:p.Arg1121Gly
|
|
|
NM_001382789.1:c.3352C>G
|
NP_001369718.1:p.Arg1118Gly
|
|
|
NM_001382790.1:c.3328C>G
|
NP_001369719.1:p.Arg1110Gly
|
|
|
NM_001382791.1:c.3322C>G
|
NP_001369720.1:p.Arg1108Gly
|
|
|
NM_001382792.1:c.3295C>G
|
NP_001369721.1:p.Arg1099Gly
|
|
|
NM_001382793.1:c.3289C>G
|
NP_001369722.1:p.Arg1097Gly
|
|
|
NM_001382794.1:c.3289C>G
|
NP_001369723.1:p.Arg1097Gly
|
|
|
NM_001382795.1:c.3283C>G
|
NP_001369724.1:p.Arg1095Gly
|
|
|
NM_001382796.1:c.3244C>G
|
NP_001369725.1:p.Arg1082Gly
|
|
|
NM_001382797.1:c.3232C>G
|
NP_001369726.1:p.Arg1078Gly
|
|
|
NM_001382798.1:c.3175C>G
|
NP_001369727.1:p.Arg1059Gly
|
|
|
NM_001382799.1:c.3151C>G
|
NP_001369728.1:p.Arg1051Gly
|
|
|
NM_001382800.1:c.3145C>G
|
NP_001369729.1:p.Arg1049Gly
|
|
|
NM_001382801.1:c.3127C>G
|
NP_001369730.1:p.Arg1043Gly
|
|
|
NM_001382802.1:c.3073C>G
|
NP_001369731.1:p.Arg1025Gly
|
|
|
NM_001382803.1:c.3118-223C>G
|
NP_001369732.1:n.3118-223C>G
|
|
|
NM_001382804.1:c.2503C>G
|
NP_001369733.1:p.Arg835Gly
|
|
|
NM_001382805.1:c.2380C>G
|
NP_001369734.1:p.Arg794Gly
|
|
|
NM_001382806.1:c.2293C>G
|
NP_001369735.1:p.Arg765Gly
|
|
|
NM_004448.4:c.3331C>G
MANE Select
|
NP_004439.2:p.Arg1111Gly
|
|
|
NR_110535.2:n.3569C>G
|
|
|
