| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001102651.1 | 314 | Missense Mutation | CAC,CGC | H39R | NP_001096121.1 |
| XM_006722635.3 | 314 | Intron | XP_006722698.1 | ||
| XM_011527660.2 | 314 | UTR 5 | XP_011525962.1 | ||
| XM_011527662.2 | 314 | Intron | XP_011525964.1 | ||
| XM_011527664.2 | 314 | Intron | XP_011525966.1 | ||
| XM_011527667.2 | 314 | Missense Mutation | CAC,CGC | H39R | XP_011525969.1 |
| XM_017026234.1 | 314 | Missense Mutation | CAC,CGC | H39R | XP_016881723.1 |
| XM_017026235.1 | 314 | Intron | XP_016881724.1 | ||
| XM_017026236.1 | 314 | Intron | XP_016881725.1 |