| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001303127.1 | 443 | Silent Mutation | TCA,TCT | S29S | NP_001290056.1 |
| NM_001303128.1 | 443 | Silent Mutation | TCA,TCT | S29S | NP_001290057.1 |
| NM_173650.2 | 443 | Silent Mutation | TCA,TCT | S29S | NP_775921.1 |
| XM_006711995.3 | 443 | Silent Mutation | TCA,TCT | S29S | XP_006712058.1 |
| XM_017003872.1 | 443 | Silent Mutation | TCA,TCT | S29S | XP_016859361.1 |
| XM_017003873.1 | 443 | Silent Mutation | TCA,TCT | S29S | XP_016859362.1 |
| XM_017003874.1 | 443 | Silent Mutation | TCA,TCT | S29S | XP_016859363.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318949.1 | 443 | Intron | NP_001305878.1 | ||
| NM_001318950.1 | 443 | Intron | NP_001305879.1 | ||
| NM_001318951.1 | 443 | Intron | NP_001305880.1 | ||
| NM_003459.4 | 443 | Intron | NP_003450.2 | ||
| XM_005264547.1 | 443 | Intron | XP_005264604.1 | ||
| XM_005264548.3 | 443 | Intron | XP_005264605.1 | ||
| XM_006712100.2 | 443 | Intron | XP_006712163.1 | ||
| XM_011533102.2 | 443 | Intron | XP_011531404.1 | ||
| XM_011533103.2 | 443 | Intron | XP_011531405.1 | ||
| XM_017004873.1 | 443 | Intron | XP_016860362.1 | ||
| XM_017004874.1 | 443 | Intron | XP_016860363.1 | ||
| XM_017004875.1 | 443 | Intron | XP_016860364.1 |