ENST00000489304.6:c.933G>T
|
ENSP00000512096.1:n.933G>T
|
|
ENST00000695675.1:n.2726G>T
|
|
|
ENST00000372285.8:c.*16G>T
MANE Select
|
ENSP00000361359.3:n.*16G>T
|
|
ENST00000372276.7:c.*176G>T
|
ENSP00000361350.3:n.*176G>T
|
|
ENST00000372285.7:c.*16G>T
|
ENSP00000361359.3:n.*16G>T
|
|
ENST00000466205.5:c.752G>T
|
|
|
ENST00000489304.5:n.926G>T
|
|
|
ENST00000620709.4:c.*397G>T
|
ENSP00000484074.1:n.*397G>T
|
|
NM_001250.5:c.*16G>T
|
NP_001241.1:n.*16G>T
|
|
NM_001302753.1:c.*176G>T
|
NP_001289682.1:n.*176G>T
|
|
NM_152854.3:c.*176G>T
|
NP_690593.1:n.*176G>T
|
|
NR_126502.1:n.943G>T
|
|
|
XM_005260617.2:c.*16G>T
|
XP_005260674.1:n.*16G>T
|
|
XM_005260619.2:c.*16G>T
|
XP_005260676.1:n.*16G>T
|
|
NM_001322421.1:c.*16G>T
|
NP_001309350.1:n.*16G>T
|
|
NM_001322422.1:c.*16G>T
|
NP_001309351.1:n.*16G>T
|
|
NM_001362758.1:c.*176G>T
|
NP_001349687.1:n.*176G>T
|
|
NR_136327.1:n.846G>T
|
|
|
XM_005260619.3:c.*16G>T
|
XP_005260676.1:n.*16G>T
|
|
XM_017028135.1:c.885G>T
|
XP_016883624.1:p.Gln295His
|
|
XM_017028136.1:c.783G>T
|
XP_016883625.1:p.Gln261His
|
|
NM_001250.6:c.*16G>T
MANE Select
|
NP_001241.1:n.*16G>T
|
|
NM_001302753.2:c.*176G>T
|
NP_001289682.1:n.*176G>T
|
|
NM_001322421.2:c.*16G>T
|
NP_001309350.1:n.*16G>T
|
|
NM_001322422.2:c.*16G>T
|
NP_001309351.1:n.*16G>T
|
|
NM_001362758.2:c.*176G>T
|
NP_001349687.1:n.*176G>T
|
|
NM_152854.4:c.*176G>T
|
NP_690593.1:n.*176G>T
|
|
NR_126502.2:n.883G>T
|
|
|
NR_136327.2:n.786G>T
|
|
|