Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003447.3 | 238 | Missense Mutation | CAC,CGC | H69R | NP_003438.1 |
XM_017011258.1 | 238 | Missense Mutation | CAC,CGC | H69R | XP_016866747.1 |
XM_017011259.1 | 238 | Missense Mutation | CAC,CGC | H69R | XP_016866748.1 |
XM_017011260.1 | 238 | Missense Mutation | CAC,CGC | H69R | XP_016866749.1 |
XM_017011261.1 | 238 | Intron | XP_016866750.1 | ||
XM_017011262.1 | 238 | Missense Mutation | CAC,CGC | H69R | XP_016866751.1 |