| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321015.1 | 135 | Intron | NP_001307944.1 | ||
| NM_001482.2 | 135 | Intron | NP_001473.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001323640.1 | 135 | Missense Mutation | CCT,CTT | P9L | NP_001310569.1 |
| NM_024063.2 | 135 | Missense Mutation | CCT,CTT | P9L | NP_076968.2 |