| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256891.1 | 556 | Silent Mutation | CTG,CTT | L166L | NP_001243820.1 |
| NM_001256892.1 | 556 | Silent Mutation | CTG,CTT | L151L | NP_001243821.1 |
| NM_003130.3 | 556 | Silent Mutation | CTG,CTT | L166L | NP_003121.1 |
| NM_198901.1 | 556 | Silent Mutation | CTG,CTT | L151L | NP_944490.1 |
| XM_011516528.1 | 556 | Silent Mutation | CTG,CTT | L123L | XP_011514830.1 |