ENST00000344209.10:c.1115A>G
MANE Select
|
ENSP00000345667.5:p.His372Arg
|
|
ENST00000460554.2:n.1065A>G
|
|
|
ENST00000642615.1:c.*298A>G
|
ENSP00000495499.1:n.*298A>G
|
|
ENST00000273691.7:c.983A>G
|
ENSP00000273691.3:p.His328Arg
|
|
ENST00000344209.9:c.1115A>G
|
ENSP00000345667.5:p.His372Arg
|
|
ENST00000393631.5:c.848A>G
|
ENSP00000377251.1:p.His283Arg
|
|
ENST00000460554.1:n.1217A>G
|
|
|
ENST00000462014.1:c.1019A>G
|
ENSP00000419414.1:p.His340Arg
|
|
NM_001199799.1:c.1115A>G
|
NP_001186728.1:p.His372Arg
|
|
NM_001199800.1:c.848A>G
|
NP_001186729.1:p.His283Arg
|
|
NM_175924.3:c.983A>G
|
NP_787120.1:p.His328Arg
|
|
XM_005247389.3:c.1019A>G
|
XP_005247446.1:p.His340Arg
|
|
XM_011512738.1:c.1115A>G
|
XP_011511040.1:p.His372Arg
|
|
XM_011512739.1:c.578A>G
|
XP_011511041.1:p.His193Arg
|
|
XM_005247389.4:c.1019A>G
|
XP_005247446.1:p.His340Arg
|
|
XM_011512738.2:c.1115A>G
|
XP_011511040.1:p.His372Arg
|
|
XM_011512739.2:c.578A>G
|
XP_011511041.1:p.His193Arg
|
|
NM_001199799.2:c.1115A>G
MANE Select
|
NP_001186728.1:p.His372Arg
|
|
NM_001199800.2:c.848A>G
|
NP_001186729.1:p.His283Arg
|
|
NM_175924.4:c.983A>G
|
NP_787120.1:p.His328Arg
|
|