Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_206893.3 | 128 | Missense Mutation | CAT,CGT | H11R | NP_996776.2 |
XM_011544989.1 | 128 | Missense Mutation | CAT,CGT | H11R | XP_011543291.1 |
XM_011544991.2 | 128 | Intron | XP_011543293.1 |