| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281987.1 | 3400 | Missense Mutation | CCC,TCC | P1163S | NP_001268916.1 |
| NM_001281988.1 | 3400 | Missense Mutation | CCC,TCC | P656S | NP_001268917.1 |
| NM_144569.5 | 3400 | Missense Mutation | CCC,TCC | P1176S | NP_653170.3 |
| XM_011542413.2 | 3400 | Missense Mutation | CCC,TCC | P656S | XP_011540715.1 |
| XM_011542414.2 | 3400 | Missense Mutation | CCC,TCC | P656S | XP_011540716.1 |
| XM_017002779.1 | 3400 | Missense Mutation | CCC,TCC | P1162S | XP_016858268.1 |
| XM_017002780.1 | 3400 | Missense Mutation | CCC,TCC | P1149S | XP_016858269.1 |
| XM_017002781.1 | 3400 | Missense Mutation | CCC,TCC | P1121S | XP_016858270.1 |
| XM_017002782.1 | 3400 | Missense Mutation | CCC,TCC | P906S | XP_016858271.1 |