| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003196.2 | 1377 | Intron | NP_003187.1 | ||
| XM_006710864.1 | 1377 | UTR 3 | XP_006710927.1 | ||
| XM_011542053.2 | 1377 | Intron | XP_011540355.1 | ||
| XM_017002200.1 | 1377 | Missense Mutation | TCT,TTT | S429F | XP_016857689.1 |
| XM_017002201.1 | 1377 | Missense Mutation | TCT,TTT | S408F | XP_016857690.1 |
| XM_017002202.1 | 1377 | Missense Mutation | TCT,TTT | S408F | XP_016857691.1 |
| XM_017002203.1 | 1377 | Missense Mutation | TCT,TTT | S392F | XP_016857692.1 |
| XM_017002204.1 | 1377 | Intron | XP_016857693.1 |