| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020242.2 | 253 | Missense Mutation | CAT,CGT | H34R | NP_064627.1 |
| XM_006713264.3 | 253 | Intron | XP_006713327.1 | ||
| XM_011533964.2 | 253 | Missense Mutation | CAT,CGT | H34R | XP_011532266.1 |
| XM_017006884.1 | 253 | Missense Mutation | CAT,CGT | H34R | XP_016862373.1 |
| XM_017006885.1 | 253 | Missense Mutation | ATC,GTC | I21V | XP_016862374.1 |
| XM_017006886.1 | 253 | UTR 5 | XP_016862375.1 | ||
| XM_017006887.1 | 253 | Missense Mutation | CAT,CGT | H34R | XP_016862376.1 |
| XM_017006888.1 | 253 | Intron | XP_016862377.1 | ||
| XM_017006889.1 | 253 | Missense Mutation | CAT,CGT | H34R | XP_016862378.1 |
| XM_017006890.1 | 253 | Intron | XP_016862379.1 |