Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001313915.1 | 3565 | Missense Mutation | CGC,CTC | R937L | NP_001300844.1 |
NM_004836.6 | 3565 | Missense Mutation | CGC,CTC | R1088L | NP_004827.4 |
XM_017005376.1 | 3565 | Missense Mutation | CGC,CTC | R860L | XP_016860865.1 |