ENST00000215882.10:c.593G=
MANE Select
|
ENSP00000215882.5:p.Arg198=
|
|
ENST00000215882.9:c.593G=
|
ENSP00000215882.5:p.Arg198=
|
|
ENST00000451283.5:c.284G=
|
ENSP00000401480.1:p.Arg95=
|
|
ENST00000461267.1:n.739G=
|
|
|
ENST00000470922.5:n.735G=
|
|
|
NM_001256534.1:c.614G=
|
NP_001243463.1:p.Arg205=
|
|
NM_001287387.1:c.284G=
|
NP_001274316.1:p.Arg95=
|
|
NM_005984.4:c.593G=
|
NP_005975.1:p.Arg198=
|
|
NR_046298.2:n.644G=
|
|
|
NM_005984.5:c.593G=
MANE Select
|
NP_005975.1:p.Arg198=
|
|
NM_001256534.2:c.614G=
|
NP_001243463.1:p.Arg205=
|
|
NM_001287387.2:c.284G=
|
NP_001274316.1:p.Arg95=
|
|
NR_046298.3:n.517G=
|
|
|