Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142552.1 | 5764 | Intron | NP_001136024.1 | ||
NM_017639.3 | 5764 | Missense Mutation | CCT,GCT | P2824A | NP_060109.2 |
XM_011532045.1 | 5764 | Missense Mutation | CCT,GCT | P3279A | XP_011530347.1 |
XM_011532046.2 | 5764 | Missense Mutation | CCT,GCT | P2502A | XP_011530348.1 |
XM_011532049.2 | 5764 | Missense Mutation | CCT,GCT | P1614A | XP_011530351.1 |
XM_017008320.1 | 5764 | Intron | XP_016863809.1 |