Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001256510.1 | 298 | Missense Mutation | CTT,TTT | L13F | NP_001243439.1 |
NM_001256511.1 | 298 | Missense Mutation | CTT,TTT | L13F | NP_001243440.1 |
NM_001256512.1 | 298 | Missense Mutation | CTT,TTT | L13F | NP_001243441.1 |
NM_001256513.1 | 298 | Intron | NP_001243442.1 | ||
NM_003143.2 | 298 | Intron | NP_003134.1 | ||
XM_005250048.4 | 298 | Missense Mutation | CTT,TTT | L13F | XP_005250105.1 |
XM_005250049.4 | 298 | Missense Mutation | CTT,TTT | L13F | XP_005250106.1 |
XM_005250050.4 | 298 | Missense Mutation | CTT,TTT | L13F | XP_005250107.1 |
XM_005250051.4 | 298 | Missense Mutation | CTT,TTT | L13F | XP_005250108.1 |