| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000835.4 | 4178 | Missense Mutation | AGC,CGC | S911R | NP_000826.2 |
| NM_001278553.1 | 4178 | Intron | NP_001265482.1 | ||
| XM_006721845.3 | 4178 | Missense Mutation | AGC,CGC | S986R | XP_006721908.1 |
| XM_006721846.3 | 4178 | Missense Mutation | AGC,CGC | S985R | XP_006721909.1 |
| XM_011524686.2 | 4178 | Missense Mutation | AGC,CGC | S1014R | XP_011522988.1 |
| XM_011524687.2 | 4178 | Missense Mutation | AGC,CGC | S1007R | XP_011522989.1 |
| XM_011524688.2 | 4178 | Missense Mutation | AGC,CGC | S994R | XP_011522990.1 |
| XM_011524689.2 | 4178 | Missense Mutation | AGC,CGC | S940R | XP_011522991.1 |
| XM_011524692.2 | 4178 | Intron | XP_011522994.1 | ||
| XM_017024544.1 | 4178 | Missense Mutation | AGC,CGC | S1015R | XP_016880033.1 |