| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145208.1 | 1391 | Intron | NP_001138680.1 | ||
| NM_018369.2 | 1391 | Missense Mutation | TAT,TGT | Y442C | NP_060839.2 |
| XM_011543509.2 | 1391 | Missense Mutation | TAT,TGT | Y427C | XP_011541811.1 |
| XM_011543510.2 | 1391 | Intron | XP_011541812.1 | ||
| XM_017009629.1 | 1391 | Intron | XP_016865118.1 |