Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001281303.1 | 1537 | Silent Mutation | CCA,CCG | P467P | NP_001268232.1 |
NM_006415.3 | 1537 | UTR 3 | NP_006406.1 | ||
NM_178324.2 | 1537 | Intron | NP_847894.1 | ||
XM_011518138.2 | 1537 | Intron | XP_011516440.1 | ||
XM_011518139.2 | 1537 | UTR 3 | XP_011516441.1 | ||
XM_017014200.1 | 1537 | UTR 3 | XP_016869689.1 | ||
XM_017014201.1 | 1537 | UTR 3 | XP_016869690.1 | ||
XM_017014202.1 | 1537 | UTR 3 | XP_016869691.1 |