Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145734.2 | 1537 | Missense Mutation | GCT,TCT | A454S | NP_001139206.2 |
NM_001170402.1 | 1537 | Missense Mutation | GCT,TCT | A496S | NP_001163873.1 |
NM_152623.2 | 1537 | Missense Mutation | GCT,TCT | A492S | NP_689836.2 |
XM_011543218.2 | 1537 | Intron | XP_011541520.1 |