| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039127.5 | 1073 | Silent Mutation | CTG,CTT | L85L | NP_001034216.2 |
| NM_001289930.1 | 1073 | Silent Mutation | CTG,CTT | L53L | NP_001276859.1 |
| NM_001289931.1 | 1073 | Intron | NP_001276860.1 | ||
| XM_017007979.1 | 1073 | Intron | XP_016863468.1 | ||
| XM_017007980.1 | 1073 | Silent Mutation | CTG,CTT | L53L | XP_016863469.1 |
| XM_017007981.1 | 1073 | Silent Mutation | CTG,CTT | L26L | XP_016863470.1 |