| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001287516.1 | 407 | Missense Mutation | CCC,CGC | P16R | NP_001274445.1 |
| NM_001287517.1 | 407 | Intron | NP_001274446.1 | ||
| NM_001287518.1 | 407 | Missense Mutation | CCC,CGC | P16R | NP_001274447.1 |
| NM_001287519.1 | 407 | Intron | NP_001274448.1 | ||
| NM_001287520.1 | 407 | UTR 5 | NP_001274449.1 | ||
| NM_001287522.1 | 407 | UTR 5 | NP_001274451.1 | ||
| NM_001287524.1 | 407 | Intron | NP_001274453.1 | ||
| NM_004358.4 | 407 | Intron | NP_004349.1 | ||
| NM_021872.3 | 407 | Missense Mutation | CCC,CGC | P80R | NP_068658.1 |
| NM_021873.3 | 407 | Missense Mutation | CCC,CGC | P80R | NP_068659.1 |