ENST00000215882.10:c.846C>G
MANE Select
|
ENSP00000215882.5:p.Arg282=
|
|
ENST00000215882.9:c.846C>G
|
ENSP00000215882.5:p.Arg282=
|
|
ENST00000451283.5:c.537C>G
|
ENSP00000401480.1:p.Arg179=
|
|
ENST00000470922.5:n.988C>G
|
|
|
NM_001256534.1:c.867C>G
|
NP_001243463.1:p.Arg289=
|
|
NM_001287387.1:c.537C>G
|
NP_001274316.1:p.Arg179=
|
|
NM_005984.4:c.846C>G
|
NP_005975.1:p.Arg282=
|
|
NR_046298.2:n.897C>G
|
|
|
NM_005984.5:c.846C>G
MANE Select
|
NP_005975.1:p.Arg282=
|
|
NM_001256534.2:c.867C>G
|
NP_001243463.1:p.Arg289=
|
|
NM_001287387.2:c.537C>G
|
NP_001274316.1:p.Arg179=
|
|
NR_046298.3:n.770C>G
|
|
|