ENST00000269571.10:c.3641G>C
MANE Select
|
ENSP00000269571.4:p.Ser1214Thr
|
|
ENST00000269571.9:c.3641G>C
|
ENSP00000269571.4:p.Ser1214Thr
|
|
ENST00000406381.6:c.3551G>C
|
ENSP00000385185.2:p.Ser1184Thr
|
|
ENST00000445658.6:c.2813G>C
|
ENSP00000404047.2:p.Ser938Thr
|
|
ENST00000541774.5:c.3596G>C
|
ENSP00000446466.1:p.Ser1199Thr
|
|
ENST00000578373.5:c.*3431G>C
|
ENSP00000463427.1:n.*3431G>C
|
|
ENST00000584450.5:c.*220G>C
|
ENSP00000463714.1:n.*220G>C
|
|
ENST00000584601.5:c.3551G>C
|
ENSP00000462438.1:p.Ser1184Thr
|
|
NM_001005862.2:c.3551G>C , LRG_724t1:c.3551G>C
|
NP_001005862.1:p.Ser1184Thr
|
|
NM_001289936.1:c.3596G>C , LRG_724t4:c.3596G>C
|
NP_001276865.1:p.Ser1199Thr
|
|
NM_001289937.1:c.*220G>C
|
NP_001276866.1:n.*220G>C
|
|
NM_004448.3:c.3641G>C , LRG_724t2:c.3641G>C
|
NP_004439.2:p.Ser1214Thr
|
|
NR_110535.1:n.3965G>C
|
|
|
XM_024450641.1:c.3779G>C
|
XP_024306409.1:p.Ser1260Thr
|
|
XM_024450642.1:c.3734G>C
|
XP_024306410.1:p.Ser1245Thr
|
|
XM_024450643.1:c.3689G>C
|
XP_024306411.1:p.Ser1230Thr
|
|
NM_001005862.3:c.3551G>C
|
NP_001005862.1:p.Ser1184Thr
|
|
NM_001289936.2:c.3596G>C
|
NP_001276865.1:p.Ser1199Thr
|
|
NM_001289937.2:c.*220G>C
|
NP_001276866.1:n.*220G>C
|
|
NM_001382782.1:c.3551G>C
|
NP_001369711.1:p.Ser1184Thr
|
|
NM_001382783.1:c.3551G>C
|
NP_001369712.1:p.Ser1184Thr
|
|
NM_001382784.1:c.3758G>C
|
NP_001369713.1:p.Ser1253Thr
|
|
NM_001382785.1:c.3743G>C
|
NP_001369714.1:p.Ser1248Thr
|
|
NM_001382786.1:c.3722G>C
|
NP_001369715.1:p.Ser1241Thr
|
|
NM_001382787.1:c.3716G>C
|
NP_001369716.1:p.Ser1239Thr
|
|
NM_001382788.1:c.3671G>C
|
NP_001369717.1:p.Ser1224Thr
|
|
NM_001382789.1:c.3662G>C
|
NP_001369718.1:p.Ser1221Thr
|
|
NM_001382790.1:c.3638G>C
|
NP_001369719.1:p.Ser1213Thr
|
|
NM_001382791.1:c.3632G>C
|
NP_001369720.1:p.Ser1211Thr
|
|
NM_001382792.1:c.3605G>C
|
NP_001369721.1:p.Ser1202Thr
|
|
NM_001382793.1:c.3599G>C
|
NP_001369722.1:p.Ser1200Thr
|
|
NM_001382794.1:c.3599G>C
|
NP_001369723.1:p.Ser1200Thr
|
|
NM_001382795.1:c.3593G>C
|
NP_001369724.1:p.Ser1198Thr
|
|
NM_001382796.1:c.3554G>C
|
NP_001369725.1:p.Ser1185Thr
|
|
NM_001382797.1:c.3542G>C
|
NP_001369726.1:p.Ser1181Thr
|
|
NM_001382798.1:c.3485G>C
|
NP_001369727.1:p.Ser1162Thr
|
|
NM_001382799.1:c.3461G>C
|
NP_001369728.1:p.Ser1154Thr
|
|
NM_001382800.1:c.3455G>C
|
NP_001369729.1:p.Ser1152Thr
|
|
NM_001382801.1:c.3437G>C
|
NP_001369730.1:p.Ser1146Thr
|
|
NM_001382802.1:c.3383G>C
|
NP_001369731.1:p.Ser1128Thr
|
|
NM_001382803.1:c.*220G>C
|
NP_001369732.1:n.*220G>C
|
|
NM_001382804.1:c.2813G>C
|
NP_001369733.1:p.Ser938Thr
|
|
NM_001382805.1:c.2690G>C
|
NP_001369734.1:p.Ser897Thr
|
|
NM_001382806.1:c.2603G>C
|
NP_001369735.1:p.Ser868Thr
|
|
NM_004448.4:c.3641G>C
MANE Select
|
NP_004439.2:p.Ser1214Thr
|
|
NR_110535.2:n.3879G>C
|
|
|