| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_057749.2 | 1492 | Missense Mutation | CAT,TAT | H355Y | NP_477097.1 |
| XM_011517366.2 | 1492 | Intron | XP_011515668.1 | ||
| XM_017013957.1 | 1492 | Missense Mutation | CAT,TAT | H355Y | XP_016869446.1 |
| XM_017013958.1 | 1492 | Missense Mutation | CAT,TAT | H355Y | XP_016869447.1 |
| XM_017013959.1 | 1492 | Missense Mutation | CAT,TAT | H355Y | XP_016869448.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017864.3 | 1492 | Intron | NP_060334.2 | ||
| XM_017013616.1 | 1492 | Intron | XP_016869105.1 | ||
| XM_017013617.1 | 1492 | Intron | XP_016869106.1 | ||
| XM_017013618.1 | 1492 | UTR 3 | XP_016869107.1 | ||
| XM_017013619.1 | 1492 | UTR 3 | XP_016869108.1 |