Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001206646.1 | 259 | Missense Mutation | CCT,CTT | P52L | NP_001193575.1 |
NM_001206647.1 | 259 | Missense Mutation | CCT,CTT | P52L | NP_001193576.1 |
NM_001206648.1 | 259 | Missense Mutation | CCT,CTT | P52L | NP_001193577.1 |
NM_020642.3 | 259 | Missense Mutation | CCT,CTT | P52L | NP_065693.2 |
XM_017018011.1 | 259 | Missense Mutation | CCT,CTT | P52L | XP_016873500.1 |
XM_017018012.1 | 259 | Missense Mutation | CCT,CTT | P52L | XP_016873501.1 |