Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321829.1 | 2258 | Missense Mutation | CAT,CGT | H883R | NP_001308758.1 |
NM_018017.3 | 2258 | Missense Mutation | CAT,CGT | H883R | NP_060487.2 |
NM_153249.1 | 2258 | Intron | NP_694981.1 | ||
XM_011539915.2 | 2258 | Missense Mutation | CAT,CGT | H636R | XP_011538217.1 |
XM_011539916.2 | 2258 | Intron | XP_011538218.1 |