Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001244638.1 | 653 | Intron | NP_001231567.1 | ||
NM_032199.2 | 653 | Missense Mutation | ACC,AGC | T66S | NP_115575.1 |
XM_011540262.1 | 653 | Missense Mutation | ACC,AGC | T66S | XP_011538564.1 |
XM_017016765.1 | 653 | Intron | XP_016872254.1 |