| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000898.4 | 1380 | Missense Mutation | CCC,CGC | P415R | NP_000889.3 |
| XM_005272608.3 | 1380 | Missense Mutation | CCC,CGC | P399R | XP_005272665.1 |
| XM_017029523.1 | 1380 | Missense Mutation | CCC,CGC | P399R | XP_016885012.1 |
| XM_017029524.1 | 1380 | Missense Mutation | CCC,CGC | P399R | XP_016885013.1 |