Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001254.3 | 621 | Missense Mutation | CAT,CGT | H69R | NP_001245.1 |
XM_011525541.1 | 621 | Missense Mutation | CAT,CGT | H69R | XP_011523843.1 |
XM_011525542.1 | 621 | Missense Mutation | CAT,CGT | H69R | XP_011523844.1 |