ENST00000344209.10:c.1123G>C
MANE Select
|
ENSP00000345667.5:p.Asp375His
|
|
ENST00000460554.2:n.1073G>C
|
|
|
ENST00000642615.1:c.*306G>C
|
ENSP00000495499.1:n.*306G>C
|
|
ENST00000273691.7:c.991G>C
|
ENSP00000273691.3:p.Asp331His
|
|
ENST00000344209.9:c.1123G>C
|
ENSP00000345667.5:p.Asp375His
|
|
ENST00000393631.5:c.856G>C
|
ENSP00000377251.1:p.Asp286His
|
|
ENST00000460554.1:n.1225G>C
|
|
|
ENST00000462014.1:c.1027G>C
|
ENSP00000419414.1:p.Asp343His
|
|
NM_001199799.1:c.1123G>C
|
NP_001186728.1:p.Asp375His
|
|
NM_001199800.1:c.856G>C
|
NP_001186729.1:p.Asp286His
|
|
NM_175924.3:c.991G>C
|
NP_787120.1:p.Asp331His
|
|
XM_005247389.3:c.1027G>C
|
XP_005247446.1:p.Asp343His
|
|
XM_011512738.1:c.1123G>C
|
XP_011511040.1:p.Asp375His
|
|
XM_011512739.1:c.586G>C
|
XP_011511041.1:p.Asp196His
|
|
XM_005247389.4:c.1027G>C
|
XP_005247446.1:p.Asp343His
|
|
XM_011512738.2:c.1123G>C
|
XP_011511040.1:p.Asp375His
|
|
XM_011512739.2:c.586G>C
|
XP_011511041.1:p.Asp196His
|
|
NM_001199799.2:c.1123G>C
MANE Select
|
NP_001186728.1:p.Asp375His
|
|
NM_001199800.2:c.856G>C
|
NP_001186729.1:p.Asp286His
|
|
NM_175924.4:c.991G>C
|
NP_787120.1:p.Asp331His
|
|