ENST00000344209.10:c.1088A>T
MANE Select
|
ENSP00000345667.5:p.Asp363Val
|
|
ENST00000460554.2:n.1038A>T
|
|
|
ENST00000642615.1:c.*271A>T
|
ENSP00000495499.1:n.*271A>T
|
|
ENST00000273691.7:c.956A>T
|
ENSP00000273691.3:p.Asp319Val
|
|
ENST00000344209.9:c.1088A>T
|
ENSP00000345667.5:p.Asp363Val
|
|
ENST00000393631.5:c.821A>T
|
ENSP00000377251.1:p.Asp274Val
|
|
ENST00000460554.1:n.1190A>T
|
|
|
ENST00000462014.1:c.992A>T
|
ENSP00000419414.1:p.Asp331Val
|
|
NM_001199799.1:c.1088A>T
|
NP_001186728.1:p.Asp363Val
|
|
NM_001199800.1:c.821A>T
|
NP_001186729.1:p.Asp274Val
|
|
NM_175924.3:c.956A>T
|
NP_787120.1:p.Asp319Val
|
|
XM_005247389.3:c.992A>T
|
XP_005247446.1:p.Asp331Val
|
|
XM_011512738.1:c.1088A>T
|
XP_011511040.1:p.Asp363Val
|
|
XM_011512739.1:c.551A>T
|
XP_011511041.1:p.Asp184Val
|
|
XM_005247389.4:c.992A>T
|
XP_005247446.1:p.Asp331Val
|
|
XM_011512738.2:c.1088A>T
|
XP_011511040.1:p.Asp363Val
|
|
XM_011512739.2:c.551A>T
|
XP_011511041.1:p.Asp184Val
|
|
NM_001199799.2:c.1088A>T
MANE Select
|
NP_001186728.1:p.Asp363Val
|
|
NM_001199800.2:c.821A>T
|
NP_001186729.1:p.Asp274Val
|
|
NM_175924.4:c.956A>T
|
NP_787120.1:p.Asp319Val
|
|