| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142503.2 | 262 | Silent Mutation | TGC,TGT | C16C | NP_001135975.1 |
| NM_001142504.2 | 262 | Intron | NP_001135976.1 | ||
| NM_014725.4 | 262 | UTR 5 | NP_055540.2 | ||
| XM_005262314.4 | 262 | Silent Mutation | TGC,TGT | C16C | XP_005262371.1 |
| XM_005262315.3 | 262 | Intron | XP_005262372.1 | ||
| XM_011531069.2 | 262 | Intron | XP_011529371.1 | ||
| XM_011531070.2 | 262 | Intron | XP_011529372.1 |