| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001127691.2 | 1121 | Intron | NP_001121163.1 | ||
| NM_001282867.1 | 1121 | Missense Mutation | AGC,GGC | S189G | NP_001269796.1 |
| NM_001282868.1 | 1121 | Intron | NP_001269797.1 | ||
| NM_001282869.1 | 1121 | Missense Mutation | AGC,GGC | S355G | NP_001269798.1 |
| NM_001282870.1 | 1121 | Missense Mutation | AGC,GGC | S355G | NP_001269799.1 |
| NM_001282871.1 | 1121 | Missense Mutation | AGC,GGC | S355G | NP_001269800.1 |
| NM_001282872.1 | 1121 | Missense Mutation | AGC,GGC | S355G | NP_001269801.1 |
| NM_016124.4 | 1121 | Missense Mutation | AGC,GGC | S355G | NP_057208.2 |
| XM_017002015.1 | 1121 | Intron | XP_016857504.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321772.1 | 1121 | Intron | NP_001308701.1 | ||
| NM_020317.4 | 1121 | Intron | NP_064713.3 | ||
| XM_011541797.1 | 1121 | Intron | XP_011540099.1 |