Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001040439.1 | 400 | Intron | NP_001035529.1 | ||
NM_001318852.1 | 400 | Intron | NP_001305781.1 | ||
NM_015133.4 | 400 | Intron | NP_055948.2 | ||
XM_005255190.2 | 400 | Intron | XP_005255247.1 | ||
XM_006720869.2 | 400 | Intron | XP_006720932.1 | ||
XM_011522429.2 | 400 | Intron | XP_011520731.1 | ||
XM_011522430.2 | 400 | Intron | XP_011520732.1 | ||
XM_011522431.2 | 400 | Intron | XP_011520733.1 | ||
XM_011522432.2 | 400 | Intron | XP_011520734.1 | ||
XM_011522433.2 | 400 | Intron | XP_011520735.1 | ||
XM_017023079.1 | 400 | Intron | XP_016878568.1 | ||
XM_017023080.1 | 400 | Intron | XP_016878569.1 | ||
XM_017023081.1 | 400 | Intron | XP_016878570.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001300900.1 | 400 | Intron | NP_001287829.1 | ||
NM_023936.1 | 400 | Intron | NP_076425.1 | ||
XM_017023595.1 | 400 | Intron | XP_016879084.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002513.2 | 400 | Missense Mutation | GCC,TCC | A60S | NP_002504.2 |
XM_005255332.4 | 400 | Missense Mutation | GCC,TCC | A60S | XP_005255389.1 |
XM_011522503.2 | 400 | Silent Mutation | CGG,CGT | R63R | XP_011520805.1 |
XM_011522504.2 | 400 | Silent Mutation | CGG,CGT | R63R | XP_011520806.1 |