| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039780.3 | 636 | Missense Mutation | CGC,CTC | R180L | NP_001034869.1 |
| NM_001287252.1 | 636 | Missense Mutation | CGC,CTC | R180L | NP_001274181.1 |
| NM_001287253.1 | 636 | Missense Mutation | CGC,CTC | R181L | NP_001274182.1 |
| XM_017009725.1 | 636 | Missense Mutation | CGC,CTC | R181L | XP_016865214.1 |