Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018207.2 | 2017 | Missense Mutation | GCC,GTC | A460V | NP_060677.2 |
XM_011541705.2 | 2017 | Missense Mutation | GCC,GTC | A339V | XP_011540007.1 |
XM_017001629.1 | 2017 | Missense Mutation | GCC,GTC | A540V | XP_016857118.1 |
XM_017001630.1 | 2017 | Missense Mutation | GCC,GTC | A529V | XP_016857119.1 |
XM_017001631.1 | 2017 | Intron | XP_016857120.1 |