| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_173685.2 | 390 | Missense Mutation | GCT,TCT | A42S | NP_775956.1 |
| XM_005250875.2 | 390 | Missense Mutation | GCT,TCT | A42S | XP_005250932.1 |
| XM_005250876.4 | 390 | Missense Mutation | GCT,TCT | A42S | XP_005250933.1 |
| XM_011516974.2 | 390 | Missense Mutation | GCT,TCT | A42S | XP_011515276.1 |
| XM_011516975.1 | 390 | Missense Mutation | GCT,TCT | A42S | XP_011515277.1 |
| XM_017013330.1 | 390 | Intron | XP_016868819.1 | ||
| XM_017013331.1 | 390 | Missense Mutation | GCT,TCT | A42S | XP_016868820.1 |
| XM_017013332.1 | 390 | Intron | XP_016868821.1 | ||
| XM_017013333.1 | 390 | UTR 5 | XP_016868822.1 | ||
| XM_017013334.1 | 390 | Intron | XP_016868823.1 |