Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001136109.1 | 723 | Missense Mutation | CGC,TGC | R315C | NP_001129581.1 |
NM_001136110.1 | 723 | Missense Mutation | CGC,TGC | R231C | NP_001129582.1 |
NM_001136112.1 | 723 | Missense Mutation | CGC,TGC | R386C | NP_001129584.1 |
NM_004347.3 | 723 | Missense Mutation | CGC,TGC | R373C | NP_004338.3 |
XM_011543021.2 | 723 | Intron | XP_011541323.1 |