| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004790.4 | 1756 | Missense Mutation | GTG,TTG | V475L | NP_004781.2 |
| NM_153276.2 | 1756 | Missense Mutation | GTG,TTG | V475L | NP_695008.1 |
| NM_153277.2 | 1756 | Intron | NP_695009.1 | ||
| NM_153278.2 | 1756 | Intron | NP_695010.1 | ||
| XM_017018562.1 | 1756 | Missense Mutation | GTG,TTG | V476L | XP_016874051.1 |