Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001281450.1 | 1211 | Missense Mutation | CAC,CGC | H361R | NP_001268379.1 |
NM_001281451.1 | 1211 | Missense Mutation | CAC,CGC | H362R | NP_001268380.1 |
NM_178125.3 | 1211 | Missense Mutation | CAC,CGC | H362R | NP_835226.2 |
XM_011515787.1 | 1211 | Intron | XP_011514089.1 | ||
XM_011515788.2 | 1211 | Missense Mutation | CAC,CGC | H153R | XP_011514090.1 |
XM_011515789.2 | 1211 | Missense Mutation | CAC,CGC | H361R | XP_011514091.2 |