ENST00000489304.6:c.935A>T
|
ENSP00000512096.1:n.935A>T
|
|
ENST00000695675.1:n.2728A>T
|
|
|
ENST00000372285.8:c.*18A>T
MANE Select
|
ENSP00000361359.3:n.*18A>T
|
|
ENST00000372276.7:c.*178A>T
|
ENSP00000361350.3:n.*178A>T
|
|
ENST00000372285.7:c.*18A>T
|
ENSP00000361359.3:n.*18A>T
|
|
ENST00000466205.5:c.754A>T
|
|
|
ENST00000489304.5:n.928A>T
|
|
|
ENST00000620709.4:c.*399A>T
|
ENSP00000484074.1:n.*399A>T
|
|
NM_001250.5:c.*18A>T
|
NP_001241.1:n.*18A>T
|
|
NM_001302753.1:c.*178A>T
|
NP_001289682.1:n.*178A>T
|
|
NM_152854.3:c.*178A>T
|
NP_690593.1:n.*178A>T
|
|
NR_126502.1:n.945A>T
|
|
|
XM_005260617.2:c.*18A>T
|
XP_005260674.1:n.*18A>T
|
|
XM_005260619.2:c.*18A>T
|
XP_005260676.1:n.*18A>T
|
|
NM_001322421.1:c.*18A>T
|
NP_001309350.1:n.*18A>T
|
|
NM_001322422.1:c.*18A>T
|
NP_001309351.1:n.*18A>T
|
|
NM_001362758.1:c.*178A>T
|
NP_001349687.1:n.*178A>T
|
|
NR_136327.1:n.848A>T
|
|
|
XM_005260619.3:c.*18A>T
|
XP_005260676.1:n.*18A>T
|
|
XM_017028135.1:c.887A>T
|
XP_016883624.1:p.Glu296Val
|
|
XM_017028136.1:c.785A>T
|
XP_016883625.1:p.Glu262Val
|
|
NM_001250.6:c.*18A>T
MANE Select
|
NP_001241.1:n.*18A>T
|
|
NM_001302753.2:c.*178A>T
|
NP_001289682.1:n.*178A>T
|
|
NM_001322421.2:c.*18A>T
|
NP_001309350.1:n.*18A>T
|
|
NM_001322422.2:c.*18A>T
|
NP_001309351.1:n.*18A>T
|
|
NM_001362758.2:c.*178A>T
|
NP_001349687.1:n.*178A>T
|
|
NM_152854.4:c.*178A>T
|
NP_690593.1:n.*178A>T
|
|
NR_126502.2:n.885A>T
|
|
|
NR_136327.2:n.788A>T
|
|
|