ENST00000215882.10:c.677T>G
MANE Select
|
ENSP00000215882.5:p.Phe226Cys
|
|
ENST00000215882.9:c.677T>G
|
ENSP00000215882.5:p.Phe226Cys
|
|
ENST00000451283.5:c.368T>G
|
ENSP00000401480.1:p.Phe123Cys
|
|
ENST00000470922.5:n.819T>G
|
|
|
NM_001256534.1:c.698T>G
|
NP_001243463.1:p.Phe233Cys
|
|
NM_001287387.1:c.368T>G
|
NP_001274316.1:p.Phe123Cys
|
|
NM_005984.4:c.677T>G
|
NP_005975.1:p.Phe226Cys
|
|
NR_046298.2:n.728T>G
|
|
|
NM_005984.5:c.677T>G
MANE Select
|
NP_005975.1:p.Phe226Cys
|
|
NM_001256534.2:c.698T>G
|
NP_001243463.1:p.Phe233Cys
|
|
NM_001287387.2:c.368T>G
|
NP_001274316.1:p.Phe123Cys
|
|
NR_046298.3:n.601T>G
|
|
|