| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001159484.1 | 5502 | Silent Mutation | TCC,TCT | S1658S | NP_001152956.1 |
| NM_207308.2 | 5502 | Silent Mutation | TCC,TCT | S1810S | NP_997191.2 |
| XM_011510122.1 | 5502 | Silent Mutation | TCC,TCT | S1766S | XP_011508424.1 |
| XM_011510123.1 | 5502 | Silent Mutation | TCC,TCT | S1757S | XP_011508425.1 |
| XM_011510124.1 | 5502 | Missense Mutation | CCT,CTT | P1742L | XP_011508426.1 |
| XM_017002788.1 | 5502 | Intron | XP_016858277.1 | ||
| XM_017002789.1 | 5502 | Intron | XP_016858278.1 |