Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005583.4 | 1910 | Missense Mutation | CCC,GCC | P235A | NP_005574.2 |
XM_005259912.3 | 1910 | Missense Mutation | CCC,GCC | P161A | XP_005259969.1 |
XM_017026816.1 | 1910 | Missense Mutation | CCC,GCC | P306A | XP_016882305.1 |
XM_017026817.1 | 1910 | Missense Mutation | CCC,GCC | P257A | XP_016882306.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271043.2 | 1910 | Intron | NP_001257972.1 | ||
NM_001271044.2 | 1910 | Intron | NP_001257973.1 | ||
NM_002501.3 | 1910 | Intron | NP_002492.2 | ||
XM_005259917.4 | 1910 | Intron | XP_005259974.1 | ||
XM_005259918.4 | 1910 | Intron | XP_005259975.1 | ||
XM_005259919.3 | 1910 | Intron | XP_005259976.1 | ||
XM_005259920.3 | 1910 | Intron | XP_005259977.1 | ||
XM_006722760.2 | 1910 | Intron | XP_006722823.1 | ||
XM_011528040.1 | 1910 | Intron | XP_011526342.1 | ||
XM_017026837.1 | 1910 | Intron | XP_016882326.1 |