| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_207327.4 | 716 | Silent Mutation | GCC,GCT | A96A | NP_997210.3 |
| XM_011529960.1 | 716 | Missense Mutation | CTT,TTT | L98F | XP_011528262.1 |
| XM_011529962.2 | 716 | Missense Mutation | CTT,TTT | L98F | XP_011528264.1 |
| XM_011529963.1 | 716 | Intron | XP_011528265.1 | ||
| XM_011529964.1 | 716 | Intron | XP_011528266.1 | ||
| XM_011529965.2 | 716 | Silent Mutation | GCC,GCT | A96A | XP_011528267.1 |