Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003146.2 | 2300 | Missense Mutation | CAC,GAC | H606D | NP_003137.1 |
XM_017018180.1 | 2300 | Missense Mutation | CAC,GAC | H740D | XP_016873669.1 |
XM_017018181.1 | 2300 | Intron | XP_016873670.1 |