Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001302623.1 | 741 | Intron | NP_001289552.1 | ||
NM_001322216.1 | 741 | Intron | NP_001309145.1 | ||
NM_001322217.1 | 741 | Intron | NP_001309146.1 | ||
NM_001322218.1 | 741 | Intron | NP_001309147.1 | ||
NM_001322219.1 | 741 | Intron | NP_001309148.1 | ||
NM_001322220.1 | 741 | Intron | NP_001309149.1 | ||
NM_001322221.1 | 741 | Intron | NP_001309150.1 | ||
NM_004941.2 | 741 | Intron | NP_004932.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001079675.2 | 741 | Missense Mutation | CCG,CTG | P433L | NP_001073143.1 |
NM_001261437.1 | 741 | Missense Mutation | CCG,CTG | P394L | NP_001248366.1 |
NM_001261438.1 | 741 | Missense Mutation | CCG,CTG | P394L | NP_001248367.1 |
NM_001261439.1 | 741 | Missense Mutation | CCG,CTG | P156L | NP_001248368.1 |
NM_001986.2 | 741 | Missense Mutation | CCG,CTG | P433L | NP_001977.1 |
XM_011524514.1 | 741 | Missense Mutation | CCG,CTG | P170L | XP_011522816.1 |
XM_017024349.1 | 741 | Missense Mutation | CCG,CTG | P428L | XP_016879838.1 |