Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001306188.1 | 696 | Missense Mutation | CAT,CGT | H80R | NP_001293117.1 |
NM_019556.2 | 696 | Missense Mutation | CAT,CGT | H80R | NP_062456.1 |
XM_011531366.2 | 696 | Missense Mutation | CAT,CGT | H80R | XP_011529668.1 |
XM_017029653.1 | 696 | Missense Mutation | CAT,CGT | H80R | XP_016885142.1 |
XM_017029654.1 | 696 | Missense Mutation | CAT,CGT | H80R | XP_016885143.1 |