Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001302961.1 | 607 | Missense Mutation | CGC,TGC | R108C | NP_001289890.1 |
NM_004917.4 | 607 | Missense Mutation | CGC,TGC | R203C | NP_004908.4 |
XM_005259441.4 | 607 | Missense Mutation | CGC,TGC | R108C | XP_005259498.2 |
XM_011527545.2 | 607 | Intron | XP_011525847.1 | ||
XM_011527546.2 | 607 | Intron | XP_011525848.1 |