| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_058004.3 | 139 | Intron | NP_477352.3 | ||
| XM_005261634.1 | 139 | Intron | XP_005261691.1 | ||
| XM_005261635.1 | 139 | Intron | XP_005261692.1 | ||
| XM_011530226.1 | 139 | Intron | XP_011528528.1 | ||
| XM_011530228.2 | 139 | Intron | XP_011528530.1 | ||
| XM_017028829.1 | 139 | Intron | XP_016884318.1 | ||
| XM_017028830.1 | 139 | Intron | XP_016884319.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000185.3 | 139 | Silent Mutation | CCA,CCG | P24P | NP_000176.2 |