| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001001933.1 | 135 | Missense Mutation | CGC,CTC | R27L | NP_001001933.1 |
| NM_001256114.1 | 135 | Missense Mutation | CGC,CTC | R17L | NP_001243043.1 |
| XM_017001316.1 | 135 | Missense Mutation | CGC,CTC | R17L | XP_016856805.1 |
| XM_017001317.1 | 135 | Missense Mutation | CGC,CTC | R17L | XP_016856806.1 |