ENST00000489304.6:c.917A>G
|
ENSP00000512096.1:n.917A>G
|
|
ENST00000695675.1:n.2710A>G
|
|
|
ENST00000372285.8:c.834A>G
MANE Select
|
ENSP00000361359.3:p.Ter278Trp
|
|
ENST00000372276.7:c.*160A>G
|
ENSP00000361350.3:n.*160A>G
|
|
ENST00000372285.7:c.834A>G
|
ENSP00000361359.3:p.Ter278Trp
|
|
ENST00000466205.5:c.736A>G
|
|
|
ENST00000489304.5:n.910A>G
|
|
|
ENST00000620709.4:c.*381A>G
|
ENSP00000484074.1:n.*381A>G
|
|
NM_001250.5:c.834A>G
|
NP_001241.1:p.Ter278Trp
|
|
NM_001302753.1:c.*160A>G
|
NP_001289682.1:n.*160A>G
|
|
NM_152854.3:c.*160A>G
|
NP_690593.1:n.*160A>G
|
|
NR_126502.1:n.927A>G
|
|
|
XM_005260617.2:c.846A>G
|
XP_005260674.1:p.Ter282Trp
|
|
XM_005260619.2:c.690A>G
|
XP_005260676.1:p.Ter230Trp
|
|
XR_936660.1:n.834A>G
|
|
|
NM_001322421.1:c.846A>G
|
NP_001309350.1:p.Ter282Trp
|
|
NM_001322422.1:c.678A>G
|
NP_001309351.1:p.Ter226Trp
|
|
NM_001362758.1:c.*160A>G
|
NP_001349687.1:n.*160A>G
|
|
NR_136327.1:n.830A>G
|
|
|
XM_005260619.3:c.690A>G
|
XP_005260676.1:p.Ter230Trp
|
|
XM_017028135.1:c.869A>G
|
XP_016883624.1:p.Glu290Gly
|
|
XM_017028136.1:c.767A>G
|
XP_016883625.1:p.Glu256Gly
|
|
NM_001250.6:c.834A>G
MANE Select
|
NP_001241.1:p.Ter278Trp
|
|
NM_001302753.2:c.*160A>G
|
NP_001289682.1:n.*160A>G
|
|
NM_001322421.2:c.846A>G
|
NP_001309350.1:p.Ter282Trp
|
|
NM_001322422.2:c.678A>G
|
NP_001309351.1:p.Ter226Trp
|
|
NM_001362758.2:c.*160A>G
|
NP_001349687.1:n.*160A>G
|
|
NM_152854.4:c.*160A>G
|
NP_690593.1:n.*160A>G
|
|
NR_126502.2:n.867A>G
|
|
|
NR_136327.2:n.770A>G
|
|
|