| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243759.1 | 566 | Missense Mutation | CCC,CGC | P194R | NP_001230688.1 |
| NM_004205.4 | 566 | Missense Mutation | CCC,CGC | P437R | NP_004196.4 |
| NM_171997.2 | 566 | Missense Mutation | CCC,CGC | P228R | NP_741994.1 |
| XM_005271721.4 | 566 | Missense Mutation | CCC,CGC | P437R | XP_005271778.1 |
| XM_005271722.2 | 566 | Missense Mutation | CCC,CGC | P437R | XP_005271779.1 |
| XM_017018539.1 | 566 | Missense Mutation | CCC,CGC | P184R | XP_016874028.1 |