Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000018.3 | 1663 | Intron | NP_000009.1 | ||
NM_001033859.2 | 1663 | Intron | NP_001029031.1 | ||
NM_001270447.1 | 1663 | Intron | NP_001257376.1 | ||
NM_001270448.1 | 1663 | Intron | NP_001257377.1 | ||
XM_006721516.2 | 1663 | Intron | XP_006721579.2 | ||
XM_011523829.1 | 1663 | Intron | XP_011522131.1 | ||
XM_011523830.1 | 1663 | Intron | XP_011522132.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004422.2 | 1663 | Missense Mutation | CCC,TCC | P679S | NP_004413.1 |
XM_005256502.1 | 1663 | Missense Mutation | CCC,TCC | P675S | XP_005256559.1 |
XM_017024298.1 | 1663 | Missense Mutation | CCC,TCC | P419S | XP_016879787.1 |