| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000094.3 | 8815 | Missense Mutation | CGC,TGC | R2927C | NP_000085.1 |
| XM_011533337.1 | 8815 | Missense Mutation | CGC,TGC | R2927C | XP_011531639.1 |
| XM_017005688.1 | 8815 | Missense Mutation | CGC,TGC | R2907C | XP_016861177.1 |
| XM_017005689.1 | 8815 | Intron | XP_016861178.1 | ||
| XM_017005690.1 | 8815 | Intron | XP_016861179.1 | ||
| XM_017005691.1 | 8815 | Intron | XP_016861180.1 | ||
| XM_017005692.1 | 8815 | Intron | XP_016861181.1 |