Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001372.3 | 12913 | Missense Mutation | GCA,GGA | A4318G | NP_001363.2 |
NM_004662.2 | 12913 | Missense Mutation | GCA,GGA | A630G | NP_004653.2 |
XM_011523703.1 | 12913 | Missense Mutation | GCA,GGA | A4333G | XP_011522005.1 |
XM_017024292.1 | 12913 | Missense Mutation | GCA,GGA | A4294G | XP_016879781.1 |
XM_017024293.1 | 12913 | Missense Mutation | GCA,GGA | A3627G | XP_016879782.1 |
XM_017024294.1 | 12913 | Intron | XP_016879783.1 | ||
XM_017024295.1 | 12913 | Intron | XP_016879784.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303281.1 | 12913 | Intron | NP_001290210.1 | ||
NM_001303282.1 | 12913 | Intron | NP_001290211.1 | ||
NM_144680.3 | 12913 | Intron | NP_653281.2 | ||
XM_011524002.2 | 12913 | Intron | XP_011522304.1 | ||
XM_017025006.1 | 12913 | Intron | XP_016880495.1 | ||
XM_017025007.1 | 12913 | Intron | XP_016880496.1 | ||
XM_017025008.1 | 12913 | Intron | XP_016880497.1 | ||
XM_017025009.1 | 12913 | Intron | XP_016880498.1 | ||
XM_017025010.1 | 12913 | Intron | XP_016880499.1 | ||
XM_017025011.1 | 12913 | Intron | XP_016880500.1 |