Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001193452.1 | 531 | Missense Mutation | CAT,CGT | H166R | NP_001180381.1 |
NM_032349.3 | 531 | Missense Mutation | ATG,GTG | M143V | NP_115725.1 |
XM_005255633.4 | 531 | UTR 3 | XP_005255690.1 |