Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001267045.1 | 896 | Intron | NP_001253974.1 | ||
NM_005789.3 | 896 | Intron | NP_005780.2 | ||
NM_176863.2 | 896 | Missense Mutation | CCT,TCT | P136S | NP_789839.1 |
XM_011524177.2 | 896 | Intron | XP_011522479.1 |