Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_153703.4 | 21 | Missense Mutation | CCA,CGA | P5R | NP_714914.2 |
XM_005270457.3 | 21 | UTR 5 | XP_005270514.1 | ||
XM_011540677.2 | 21 | Intron | XP_011538979.1 | ||
XM_017000294.1 | 21 | Intron | XP_016855783.1 |