Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318878.1 | 1656 | Missense Mutation | TCG,TTG | S495L | NP_001305807.1 |
NM_001318879.1 | 1656 | Missense Mutation | TCG,TTG | S365L | NP_001305808.1 |
NM_001318880.1 | 1656 | Intron | NP_001305809.1 | ||
NM_001318881.1 | 1656 | Intron | NP_001305810.1 | ||
NM_001318882.1 | 1656 | Intron | NP_001305811.1 | ||
NM_001318883.1 | 1656 | Intron | NP_001305812.1 | ||
NM_173575.3 | 1656 | Missense Mutation | TCG,TTG | S482L | NP_775846.2 |
XM_011539688.1 | 1656 | Missense Mutation | TCG,TTG | S500L | XP_011537990.1 |
XM_011539690.2 | 1656 | Missense Mutation | TCG,TTG | S487L | XP_011537992.1 |
XM_011539693.2 | 1656 | Missense Mutation | TCG,TTG | S365L | XP_011537995.1 |
XM_011539694.1 | 1656 | Missense Mutation | TCG,TTG | S365L | XP_011537996.1 |
XM_011539695.1 | 1656 | Missense Mutation | TCG,TTG | S365L | XP_011537997.1 |
XM_011539696.1 | 1656 | Missense Mutation | TCG,TTG | S365L | XP_011537998.1 |
XM_017016100.1 | 1656 | Intron | XP_016871589.1 | ||
XM_017016101.1 | 1656 | Intron | XP_016871590.1 |