Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002848.3 | 531 | Missense Mutation | CTT,TTT | L21F | NP_002839.1 |
NM_030667.2 | 531 | Missense Mutation | CTT,TTT | L21F | NP_109592.1 |
NM_030668.2 | 531 | Intron | NP_109593.1 | ||
NM_030669.2 | 531 | Intron | NP_109594.1 | ||
NM_030670.2 | 531 | Intron | NP_109595.1 | ||
NM_030671.2 | 531 | Intron | NP_109596.1 | ||
XM_017019725.1 | 531 | Missense Mutation | CTT,TTT | L21F | XP_016875214.1 |