| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_030882.3 | 775 | Intron | NP_112092.2 | ||
| NM_145637.2 | 775 | Missense Mutation | CGT,GGT | R100G | NP_663612.2 |
| XM_011530074.1 | 775 | Intron | XP_011528376.1 | ||
| XM_011530075.1 | 775 | Intron | XP_011528377.1 | ||
| XM_011530076.2 | 775 | Intron | XP_011528378.1 | ||
| XM_011530077.2 | 775 | Intron | XP_011528379.1 | ||
| XM_011530078.1 | 775 | Intron | XP_011528380.1 | ||
| XM_017028724.1 | 775 | Intron | XP_016884213.1 |