| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_005253.3 | 978 | Missense Mutation | CCC,TCC | P6S | NP_005244.1 |
| XM_005264231.3 | 978 | Missense Mutation | CCC,TCC | P6S | XP_005264288.1 |
| XM_006711976.2 | 978 | Missense Mutation | CCC,TCC | P6S | XP_006712039.1 |
| XM_006711977.3 | 978 | Intron | XP_006712040.1 | ||
| XM_017003737.1 | 978 | Intron | XP_016859226.1 |