| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256613.1 | 483 | Missense Mutation | TCC,TTC | S6F | NP_001243542.1 |
| NM_001256614.1 | 483 | Intron | NP_001243543.1 | ||
| NM_182589.2 | 483 | Intron | NP_872395.2 | ||
| NM_198313.2 | 483 | Missense Mutation | TCC,TTC | S6F | NP_938055.1 |
| NM_198314.2 | 483 | Intron | NP_938056.1 |