| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015906.3 | 2673 | Missense Mutation | TCT,TTT | S1105F | NP_056990.3 |
| NM_033020.2 | 2673 | Missense Mutation | TCT,TTT | S1088F | NP_148980.2 |
| XM_005270936.3 | 2673 | Missense Mutation | TCT,TTT | S1129F | XP_005270993.1 |
| XM_005270937.3 | 2673 | Missense Mutation | TCT,TTT | S1112F | XP_005270994.1 |
| XM_011541568.2 | 2673 | Missense Mutation | TCT,TTT | S1128F | XP_011539870.1 |
| XM_017001452.1 | 2673 | Missense Mutation | TCT,TTT | S713F | XP_016856941.1 |
| XM_017001453.1 | 2673 | Missense Mutation | TCT,TTT | S696F | XP_016856942.1 |
| XM_017001454.1 | 2673 | Intron | XP_016856943.1 |