Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001178133.1 | 357 | Missense Mutation | GCT,TCT | A56S | NP_001171604.1 |
NM_016169.3 | 357 | Missense Mutation | GCT,TCT | A56S | NP_057253.2 |
XM_011539858.2 | 357 | Missense Mutation | GCT,TCT | A56S | XP_011538160.1 |
XM_011539860.2 | 357 | Missense Mutation | GCT,TCT | A56S | XP_011538162.1 |
XM_011539861.2 | 357 | Missense Mutation | GCT,TCT | A56S | XP_011538163.1 |
XM_011539863.2 | 357 | Intron | XP_011538165.1 | ||
XM_011539864.2 | 357 | Missense Mutation | GCT,TCT | A56S | XP_011538166.1 |
XM_017016323.1 | 357 | Intron | XP_016871812.1 |