Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005692.4 | 2149 | Missense Mutation | CCA,CTA | P632L | NP_005683.2 |
NM_007189.2 | 2149 | Intron | NP_009120.1 | ||
XM_017011639.1 | 2149 | Intron | XP_016867128.1 | ||
XM_017011640.1 | 2149 | Intron | XP_016867129.1 |