ENST00000215882.10:c.651C>G
MANE Select
|
ENSP00000215882.5:p.Pro217=
|
|
ENST00000215882.9:c.651C>G
|
ENSP00000215882.5:p.Pro217=
|
|
ENST00000451283.5:c.342C>G
|
ENSP00000401480.1:p.Pro114=
|
|
ENST00000461267.1:n.797C>G
|
|
|
ENST00000470922.5:n.793C>G
|
|
|
NM_001256534.1:c.672C>G
|
NP_001243463.1:p.Pro224=
|
|
NM_001287387.1:c.342C>G
|
NP_001274316.1:p.Pro114=
|
|
NM_005984.4:c.651C>G
|
NP_005975.1:p.Pro217=
|
|
NR_046298.2:n.702C>G
|
|
|
NM_005984.5:c.651C>G
MANE Select
|
NP_005975.1:p.Pro217=
|
|
NM_001256534.2:c.672C>G
|
NP_001243463.1:p.Pro224=
|
|
NM_001287387.2:c.342C>G
|
NP_001274316.1:p.Pro114=
|
|
NR_046298.3:n.575C>G
|
|
|