| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001174159.1 | 363 | Intron | NP_001167630.1 | ||
| NM_001174160.1 | 363 | Missense Mutation | CCA,TCA | P10S | NP_001167631.1 |
| NM_022071.3 | 363 | UTR 5 | NP_071354.2 | ||
| XM_011544610.1 | 363 | UTR 5 | XP_011542912.1 | ||
| XM_017013729.1 | 363 | Intron | XP_016869218.1 |