| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012335.3 | 3196 | Missense Mutation | CCC,TCC | P1044S | NP_036467.2 |
| XM_011528024.1 | 3196 | Missense Mutation | CCC,TCC | P1065S | XP_011526326.1 |
| XM_011528025.1 | 3196 | Missense Mutation | CCC,TCC | P1061S | XP_011526327.1 |
| XM_011528026.1 | 3196 | Missense Mutation | CCC,TCC | P1036S | XP_011526328.1 |
| XM_011528027.1 | 3196 | Missense Mutation | CCC,TCC | P1020S | XP_011526329.1 |
| XM_011528028.2 | 3196 | Intron | XP_011526330.1 | ||
| XM_017026821.1 | 3196 | Missense Mutation | CCC,TCC | P1040S | XP_016882310.1 |