| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001099436.3 | 1550 | Missense Mutation | TCT,TTT | S464F | NP_001092906.3 |
| NM_001284364.2 | 1550 | Missense Mutation | TCT,TTT | S462F | NP_001271293.2 |
| NM_001284365.2 | 1550 | Missense Mutation | TCT,TTT | S347F | NP_001271294.1 |
| XM_005254289.2 | 1550 | Missense Mutation | TCT,TTT | S475F | XP_005254346.1 |
| XM_017022068.1 | 1550 | Missense Mutation | TCT,TTT | S473F | XP_016877557.1 |
| XM_017022069.1 | 1550 | Missense Mutation | TCT,TTT | S374F | XP_016877558.1 |
| XM_017022070.1 | 1550 | Missense Mutation | TCT,TTT | S374F | XP_016877559.1 |
| XM_017022071.1 | 1550 | Missense Mutation | TCT,TTT | S372F | XP_016877560.1 |
| XM_017022072.1 | 1550 | Missense Mutation | TCT,TTT | S372F | XP_016877561.1 |