Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001302959.1 | 3904 | Intron | NP_001289888.1 | ||
NM_001302960.1 | 3904 | Intron | NP_001289889.1 | ||
NM_003977.3 | 3904 | Intron | NP_003968.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001130848.1 | 3904 | Missense Mutation | CCG,CTG | P1220L | NP_001124320.1 |
NM_004910.2 | 3904 | Missense Mutation | CCG,CTG | P1221L | NP_004901.2 |
XM_011545396.2 | 3904 | Missense Mutation | CCG,CTG | P1220L | XP_011543698.1 |
XM_017018586.1 | 3904 | Missense Mutation | CCG,CTG | P1221L | XP_016874075.1 |