Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145640.1 | 2605 | Intron | NP_001139112.1 | ||
NM_015174.1 | 2605 | Missense Mutation | GCC,GTC | A864V | NP_055989.1 |
XM_011527831.2 | 2605 | Missense Mutation | GCC,GTC | A865V | XP_011526133.1 |