| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001190799.1 | 246 | Missense Mutation | AGC,TGC | S4C | NP_001177728.1 |
| NM_001190801.1 | 246 | Intron | NP_001177730.1 | ||
| NM_014264.4 | 246 | Missense Mutation | AGC,TGC | S4C | NP_055079.3 |
| XM_005262701.2 | 246 | Missense Mutation | AGC,TGC | S4C | XP_005262758.1 |
| XM_017007662.1 | 246 | Intron | XP_016863151.1 | ||
| XM_017007663.1 | 246 | Intron | XP_016863152.1 |