| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199922.1 | 361 | UTR 5 | NP_001186851.1 | ||
| NM_170601.4 | 361 | Intron | NP_733746.1 | ||
| XM_017017930.1 | 361 | Intron | XP_016873419.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017425.3 | 361 | Missense Mutation | CCG,TCG | P2S | NP_059121.1 |
| XM_011542870.2 | 361 | Missense Mutation | CCG,TCG | P2S | XP_011541172.1 |