Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142319.1 | 2087 | Missense Mutation | TCT,TTT | S613F | NP_001135791.1 |
NM_025203.2 | 2087 | Silent Mutation | CTC,CTT | L652L | NP_079479.1 |
XM_017005029.1 | 2087 | Intron | XP_016860518.1 |