ENST00000269571.10:c.3687G>A
MANE Select
|
ENSP00000269571.4:p.Glu1229=
|
|
ENST00000269571.9:c.3687G>A
|
ENSP00000269571.4:p.Glu1229=
|
|
ENST00000406381.6:c.3597G>A
|
ENSP00000385185.2:p.Glu1199=
|
|
ENST00000445658.6:c.2859G>A
|
ENSP00000404047.2:p.Glu953=
|
|
ENST00000541774.5:c.3642G>A
|
ENSP00000446466.1:p.Glu1214=
|
|
ENST00000578373.5:c.*3477G>A
|
ENSP00000463427.1:n.*3477G>A
|
|
ENST00000584450.5:c.*266G>A
|
ENSP00000463714.1:n.*266G>A
|
|
ENST00000584601.5:c.3597G>A
|
ENSP00000462438.1:p.Glu1199=
|
|
NM_001005862.2:c.3597G>A , LRG_724t1:c.3597G>A
|
NP_001005862.1:p.Glu1199=
|
|
NM_001289936.1:c.3642G>A , LRG_724t4:c.3642G>A
|
NP_001276865.1:p.Glu1214=
|
|
NM_001289937.1:c.*266G>A
|
NP_001276866.1:n.*266G>A
|
|
NM_004448.3:c.3687G>A , LRG_724t2:c.3687G>A
|
NP_004439.2:p.Glu1229=
|
|
NR_110535.1:n.4011G>A
|
|
|
XM_024450641.1:c.3825G>A
|
XP_024306409.1:p.Glu1275=
|
|
XM_024450642.1:c.3780G>A
|
XP_024306410.1:p.Glu1260=
|
|
XM_024450643.1:c.3735G>A
|
XP_024306411.1:p.Glu1245=
|
|
NM_001005862.3:c.3597G>A
|
NP_001005862.1:p.Glu1199=
|
|
NM_001289936.2:c.3642G>A
|
NP_001276865.1:p.Glu1214=
|
|
NM_001289937.2:c.*266G>A
|
NP_001276866.1:n.*266G>A
|
|
NM_001382782.1:c.3597G>A
|
NP_001369711.1:p.Glu1199=
|
|
NM_001382783.1:c.3597G>A
|
NP_001369712.1:p.Glu1199=
|
|
NM_001382784.1:c.3804G>A
|
NP_001369713.1:p.Glu1268=
|
|
NM_001382785.1:c.3789G>A
|
NP_001369714.1:p.Glu1263=
|
|
NM_001382786.1:c.3768G>A
|
NP_001369715.1:p.Glu1256=
|
|
NM_001382787.1:c.3762G>A
|
NP_001369716.1:p.Glu1254=
|
|
NM_001382788.1:c.3717G>A
|
NP_001369717.1:p.Glu1239=
|
|
NM_001382789.1:c.3708G>A
|
NP_001369718.1:p.Glu1236=
|
|
NM_001382790.1:c.3684G>A
|
NP_001369719.1:p.Glu1228=
|
|
NM_001382791.1:c.3678G>A
|
NP_001369720.1:p.Glu1226=
|
|
NM_001382792.1:c.3651G>A
|
NP_001369721.1:p.Glu1217=
|
|
NM_001382793.1:c.3645G>A
|
NP_001369722.1:p.Glu1215=
|
|
NM_001382794.1:c.3645G>A
|
NP_001369723.1:p.Glu1215=
|
|
NM_001382795.1:c.3639G>A
|
NP_001369724.1:p.Glu1213=
|
|
NM_001382796.1:c.3600G>A
|
NP_001369725.1:p.Glu1200=
|
|
NM_001382797.1:c.3588G>A
|
NP_001369726.1:p.Glu1196=
|
|
NM_001382798.1:c.3531G>A
|
NP_001369727.1:p.Glu1177=
|
|
NM_001382799.1:c.3507G>A
|
NP_001369728.1:p.Glu1169=
|
|
NM_001382800.1:c.3501G>A
|
NP_001369729.1:p.Glu1167=
|
|
NM_001382801.1:c.3483G>A
|
NP_001369730.1:p.Glu1161=
|
|
NM_001382802.1:c.3429G>A
|
NP_001369731.1:p.Glu1143=
|
|
NM_001382803.1:c.*266G>A
|
NP_001369732.1:n.*266G>A
|
|
NM_001382804.1:c.2859G>A
|
NP_001369733.1:p.Glu953=
|
|
NM_001382805.1:c.2736G>A
|
NP_001369734.1:p.Glu912=
|
|
NM_001382806.1:c.2649G>A
|
NP_001369735.1:p.Glu883=
|
|
NM_004448.4:c.3687G>A
MANE Select
|
NP_004439.2:p.Glu1229=
|
|
NR_110535.2:n.3925G>A
|
|
|