Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_144581.1 | 2602 | Missense Mutation | AGG,AGT | R348S | NP_653182.1 |
XM_005267298.3 | 2602 | Missense Mutation | AGG,AGT | R177S | XP_005267355.1 |
XM_011536386.2 | 2602 | Intron | XP_011534688.1 | ||
XM_011536387.1 | 2602 | UTR 3 | XP_011534689.1 | ||
XM_011536388.1 | 2602 | UTR 3 | XP_011534690.1 |