ENST00000215882.10:c.549C>T
MANE Select
|
ENSP00000215882.5:p.Gly183=
|
|
ENST00000215882.9:c.549C>T
|
ENSP00000215882.5:p.Gly183=
|
|
ENST00000451283.5:c.240C>T
|
ENSP00000401480.1:p.Gly80=
|
|
ENST00000461267.1:n.695C>T
|
|
|
ENST00000470922.5:n.691C>T
|
|
|
NM_001256534.1:c.570C>T
|
NP_001243463.1:p.Gly190=
|
|
NM_001287387.1:c.240C>T
|
NP_001274316.1:p.Gly80=
|
|
NM_005984.4:c.549C>T
|
NP_005975.1:p.Gly183=
|
|
NR_046298.2:n.600C>T
|
|
|
NM_005984.5:c.549C>T
MANE Select
|
NP_005975.1:p.Gly183=
|
|
NM_001256534.2:c.570C>T
|
NP_001243463.1:p.Gly190=
|
|
NM_001287387.2:c.240C>T
|
NP_001274316.1:p.Gly80=
|
|
NR_046298.3:n.473C>T
|
|
|