ENST00000215882.10:c.865G>C
MANE Select
|
ENSP00000215882.5:p.Asp289His
|
|
ENST00000215882.9:c.865G>C
|
ENSP00000215882.5:p.Asp289His
|
|
ENST00000451283.5:c.556G>C
|
ENSP00000401480.1:p.Asp186His
|
|
ENST00000470922.5:n.1007G>C
|
|
|
NM_001256534.1:c.886G>C
|
NP_001243463.1:p.Asp296His
|
|
NM_001287387.1:c.556G>C
|
NP_001274316.1:p.Asp186His
|
|
NM_005984.4:c.865G>C
|
NP_005975.1:p.Asp289His
|
|
NR_046298.2:n.916G>C
|
|
|
NM_005984.5:c.865G>C
MANE Select
|
NP_005975.1:p.Asp289His
|
|
NM_001256534.2:c.886G>C
|
NP_001243463.1:p.Asp296His
|
|
NM_001287387.2:c.556G>C
|
NP_001274316.1:p.Asp186His
|
|
NR_046298.3:n.789G>C
|
|
|