ENST00000344209.10:c.1071T>C
MANE Select
|
ENSP00000345667.5:p.Ile357=
|
|
ENST00000460554.2:n.1021T>C
|
|
|
ENST00000642615.1:c.*254T>C
|
ENSP00000495499.1:n.*254T>C
|
|
ENST00000273691.7:c.939T>C
|
ENSP00000273691.3:p.Ile313=
|
|
ENST00000344209.9:c.1071T>C
|
ENSP00000345667.5:p.Ile357=
|
|
ENST00000393631.5:c.804T>C
|
ENSP00000377251.1:p.Ile268=
|
|
ENST00000460554.1:n.1173T>C
|
|
|
ENST00000462014.1:c.975T>C
|
ENSP00000419414.1:p.Ile325=
|
|
NM_001199799.1:c.1071T>C
|
NP_001186728.1:p.Ile357=
|
|
NM_001199800.1:c.804T>C
|
NP_001186729.1:p.Ile268=
|
|
NM_175924.3:c.939T>C
|
NP_787120.1:p.Ile313=
|
|
XM_005247389.3:c.975T>C
|
XP_005247446.1:p.Ile325=
|
|
XM_011512738.1:c.1071T>C
|
XP_011511040.1:p.Ile357=
|
|
XM_011512739.1:c.534T>C
|
XP_011511041.1:p.Ile178=
|
|
XM_005247389.4:c.975T>C
|
XP_005247446.1:p.Ile325=
|
|
XM_011512738.2:c.1071T>C
|
XP_011511040.1:p.Ile357=
|
|
XM_011512739.2:c.534T>C
|
XP_011511041.1:p.Ile178=
|
|
NM_001199799.2:c.1071T>C
MANE Select
|
NP_001186728.1:p.Ile357=
|
|
NM_001199800.2:c.804T>C
|
NP_001186729.1:p.Ile268=
|
|
NM_175924.4:c.939T>C
|
NP_787120.1:p.Ile313=
|
|