Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001193452.1 | 530 | Missense Mutation | CGT,TGT | R166C | NP_001180381.1 |
NM_032349.3 | 530 | Silent Mutation | CTC,CTT | L142L | NP_115725.1 |
XM_005255633.4 | 530 | UTR 3 | XP_005255690.1 |