| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142552.1 | 6017 | Intron | NP_001136024.1 | ||
| NM_017639.3 | 6017 | Missense Mutation | CAT,CTT | H2908L | NP_060109.2 |
| XM_011532045.1 | 6017 | Missense Mutation | CAT,CTT | H3363L | XP_011530347.1 |
| XM_011532046.2 | 6017 | Missense Mutation | CAT,CTT | H2586L | XP_011530348.1 |
| XM_011532049.2 | 6017 | Missense Mutation | CAT,CTT | H1698L | XP_011530351.1 |
| XM_017008320.1 | 6017 | Intron | XP_016863809.1 |