| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000970.4 | 800 | Intron | NP_000961.2 | ||
| NM_001024662.2 | 800 | Intron | NP_001019833.1 | ||
| NM_001320137.1 | 800 | Intron | NP_001307066.1 | ||
| NM_001320138.1 | 800 | Missense Mutation | CCT,CTT | P174L | NP_001307067.1 |
| NM_001320139.1 | 800 | Intron | NP_001307068.1 | ||
| NM_001320140.1 | 800 | Missense Mutation | CCT,CTT | P174L | NP_001307069.1 |
| NM_001320141.1 | 800 | Missense Mutation | CCT,CTT | P174L | NP_001307070.1 |
| NM_001320142.1 | 800 | Intron | NP_001307071.1 | ||
| XM_017019781.1 | 800 | Missense Mutation | CCT,CTT | P174L | XP_016875270.1 |
| XM_017019782.1 | 800 | Intron | XP_016875271.1 |