ENST00000644719.2:c.433C>T
MANE Select
|
ENSP00000496625.1:p.Gln145Ter
|
|
ENST00000418967.6:c.433C>T
|
ENSP00000408860.2:p.Gln145Ter
|
|
ENST00000435122.3:c.343C>T
|
ENSP00000415043.2:p.Gln115Ter
|
|
ENST00000462278.1:n.21C>T
|
|
|
ENST00000464325.5:n.354C>T
|
|
|
ENST00000466779.5:c.*125C>T
|
ENSP00000417321.1:n.*125C>T
|
|
ENST00000466879.5:n.484C>T
|
|
|
ENST00000469053.5:c.*125C>T
|
ENSP00000418104.1:n.*125C>T
|
|
ENST00000471671.4:c.433C>T
|
ENSP00000418561.1:p.Gln145Ter
|
|
ENST00000478281.5:c.466C>T
|
ENSP00000419572.1:p.Gln156Ter
|
|
ENST00000479074.5:n.491C>T
|
|
|
ENST00000479730.5:n.588C>T
|
|
|
ENST00000483041.5:n.602C>T
|
|
|
ENST00000486063.5:n.613C>T
|
|
|
ENST00000488465.1:n.441C>T
|
|
|
NM_000500.7:c.433C>T
|
NP_000491.4:p.Gln145Ter
|
|
NM_001128590.3:c.343C>T
|
NP_001122062.3:p.Gln115Ter
|
|
XM_011514314.1:c.28C>T
|
XP_011512616.1:p.Gln10Ter
|
|
NM_000500.9:c.433C>T
MANE Select
|
NP_000491.4:p.Gln145Ter
|
|
NM_001368143.1:c.28C>T
|
NP_001355072.1:p.Gln10Ter
|
|
NM_001368144.1:c.28C>T
|
NP_001355073.1:p.Gln10Ter
|
|
NM_001128590.4:c.343C>T
|
NP_001122062.3:p.Gln115Ter
|
|
NM_001368143.2:c.28C>T
|
NP_001355072.1:p.Gln10Ter
|
|
NM_001368144.2:c.28C>T
|
NP_001355073.1:p.Gln10Ter
|
|