ENST00000344209.10:c.1239A>C
MANE Select
|
ENSP00000345667.5:p.Ile413=
|
|
ENST00000460554.2:n.1189A>C
|
|
|
ENST00000642615.1:c.*422A>C
|
ENSP00000495499.1:n.*422A>C
|
|
ENST00000273691.7:c.1107A>C
|
ENSP00000273691.3:p.Ile369=
|
|
ENST00000344209.9:c.1239A>C
|
ENSP00000345667.5:p.Ile413=
|
|
ENST00000393631.5:c.972A>C
|
ENSP00000377251.1:p.Ile324=
|
|
ENST00000460554.1:n.1341A>C
|
|
|
ENST00000462014.1:c.1143A>C
|
ENSP00000419414.1:p.Ile381=
|
|
NM_001199799.1:c.1239A>C
|
NP_001186728.1:p.Ile413=
|
|
NM_001199800.1:c.972A>C
|
NP_001186729.1:p.Ile324=
|
|
NM_175924.3:c.1107A>C
|
NP_787120.1:p.Ile369=
|
|
XM_005247389.3:c.1143A>C
|
XP_005247446.1:p.Ile381=
|
|
XM_011512738.1:c.1239A>C
|
XP_011511040.1:p.Ile413=
|
|
XM_011512739.1:c.702A>C
|
XP_011511041.1:p.Ile234=
|
|
XM_005247389.4:c.1143A>C
|
XP_005247446.1:p.Ile381=
|
|
XM_011512738.2:c.1239A>C
|
XP_011511040.1:p.Ile413=
|
|
XM_011512739.2:c.702A>C
|
XP_011511041.1:p.Ile234=
|
|
NM_001199799.2:c.1239A>C
MANE Select
|
NP_001186728.1:p.Ile413=
|
|
NM_001199800.2:c.972A>C
|
NP_001186729.1:p.Ile324=
|
|
NM_175924.4:c.1107A>C
|
NP_787120.1:p.Ile369=
|
|