|
ENST00000477696.6:c.413A>T
|
ENSP00000512095.1:n.413A>T
|
|
|
ENST00000489304.6:c.317A>T
|
ENSP00000512096.1:p.Glu106Val
|
|
|
ENST00000695669.1:n.390A>T
|
|
|
|
ENST00000695670.1:n.297A>T
|
|
|
|
ENST00000695671.1:c.317A>T
|
ENSP00000512093.1:p.Glu106Val
|
|
|
ENST00000695672.1:n.242A>T
|
|
|
|
ENST00000695673.1:n.182A>T
|
|
|
|
ENST00000372285.8:c.317A>T
MANE Select
|
ENSP00000361359.3:p.Glu106Val
|
|
|
ENST00000372276.7:c.317A>T
|
ENSP00000361350.3:p.Glu106Val
|
|
|
ENST00000372285.7:c.317A>T
|
ENSP00000361359.3:p.Glu106Val
|
|
|
ENST00000461171.1:n.102A>T
|
|
|
|
ENST00000466205.5:c.313A>T
|
|
|
|
ENST00000477696.5:n.384A>T
|
|
|
|
ENST00000489304.5:n.310A>T
|
|
|
|
ENST00000620709.4:c.317A>T
|
ENSP00000484074.1:p.Glu106Val
|
|
|
NM_001250.5:c.317A>T
|
NP_001241.1:p.Glu106Val
|
|
|
NM_001302753.1:c.317A>T
|
NP_001289682.1:p.Glu106Val
|
|
|
NM_152854.3:c.317A>T
|
NP_690593.1:p.Glu106Val
|
|
|
NR_126502.1:n.407A>T
|
|
|
|
XM_005260617.2:c.317A>T
|
XP_005260674.1:p.Glu106Val
|
|
|
XM_005260619.2:c.317A>T
|
XP_005260676.1:p.Glu106Val
|
|
|
XM_011529109.1:c.317A>T
|
XP_011527411.1:p.Glu106Val
|
|
|
XR_936660.1:n.411A>T
|
|
|
|
NM_001322421.1:c.317A>T
|
NP_001309350.1:p.Glu106Val
|
|
|
NM_001322422.1:c.317A>T
|
NP_001309351.1:p.Glu106Val
|
|
|
NM_001362758.1:c.317A>T
|
NP_001349687.1:p.Glu106Val
|
|
|
NR_136327.1:n.407A>T
|
|
|
|
XM_005260619.3:c.317A>T
|
XP_005260676.1:p.Glu106Val
|
|
|
XM_011529109.2:c.317A>T
|
XP_011527411.1:p.Glu106Val
|
|
|
XM_017028135.1:c.317A>T
|
XP_016883624.1:p.Glu106Val
|
|
|
XM_017028136.1:c.317A>T
|
XP_016883625.1:p.Glu106Val
|
|
|
NM_001250.6:c.317A>T
MANE Select
|
NP_001241.1:p.Glu106Val
|
|
|
NM_001302753.2:c.317A>T
|
NP_001289682.1:p.Glu106Val
|
|
|
NM_001322421.2:c.317A>T
|
NP_001309350.1:p.Glu106Val
|
|
|
NM_001322422.2:c.317A>T
|
NP_001309351.1:p.Glu106Val
|
|
|
NM_001362758.2:c.317A>T
|
NP_001349687.1:p.Glu106Val
|
|
|
NM_152854.4:c.317A>T
|
NP_690593.1:p.Glu106Val
|
|
|
NR_126502.2:n.347A>T
|
|
|
|
NR_136327.2:n.347A>T
|
|
|
