Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145640.1 | 2661 | Intron | NP_001139112.1 | ||
NM_015174.1 | 2661 | Missense Mutation | ACC,GCC | T883A | NP_055989.1 |
XM_011527831.2 | 2661 | Missense Mutation | ACC,GCC | T884A | XP_011526133.1 |