| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001136499.1 | 4637 | Missense Mutation | CCG,CGG | P861R | NP_001129971.1 |
| NM_001321349.1 | 4637 | Missense Mutation | CCG,CGG | P745R | NP_001308278.1 |
| XM_011526833.2 | 4637 | Intron | XP_011525135.1 | ||
| XM_017026652.1 | 4637 | Intron | XP_016882141.1 | ||
| XM_017026653.1 | 4637 | Missense Mutation | CCG,CGG | P862R | XP_016882142.1 |
| XM_017026654.1 | 4637 | Missense Mutation | CCG,CGG | P862R | XP_016882143.1 |
| XM_017026655.1 | 4637 | Intron | XP_016882144.1 | ||
| XM_017026656.1 | 4637 | Missense Mutation | CCG,CGG | P861R | XP_016882145.1 |
| XM_017026657.1 | 4637 | Intron | XP_016882146.1 | ||
| XM_017026658.1 | 4637 | Intron | XP_016882147.1 | ||
| XM_017026659.1 | 4637 | Intron | XP_016882148.1 | ||
| XM_017026660.1 | 4637 | Intron | XP_016882149.1 | ||
| XM_017026661.1 | 4637 | Intron | XP_016882150.1 | ||
| XM_017026662.1 | 4637 | Intron | XP_016882151.1 | ||
| XM_017026663.1 | 4637 | Intron | XP_016882152.1 |