ENST00000489304.6:c.980G>C
|
ENSP00000512096.1:n.980G>C
|
|
ENST00000695675.1:n.2773G>C
|
|
|
ENST00000372285.8:c.*63G>C
MANE Select
|
ENSP00000361359.3:n.*63G>C
|
|
ENST00000372276.7:c.*223G>C
|
ENSP00000361350.3:n.*223G>C
|
|
ENST00000372285.7:c.*63G>C
|
ENSP00000361359.3:n.*63G>C
|
|
ENST00000466205.5:c.799G>C
|
|
|
ENST00000489304.5:n.973G>C
|
|
|
ENST00000620709.4:c.*444G>C
|
ENSP00000484074.1:n.*444G>C
|
|
NM_001250.5:c.*63G>C
|
NP_001241.1:n.*63G>C
|
|
NM_001302753.1:c.*223G>C
|
NP_001289682.1:n.*223G>C
|
|
NM_152854.3:c.*223G>C
|
NP_690593.1:n.*223G>C
|
|
NR_126502.1:n.990G>C
|
|
|
XM_005260617.2:c.*63G>C
|
XP_005260674.1:n.*63G>C
|
|
XM_005260619.2:c.*63G>C
|
XP_005260676.1:n.*63G>C
|
|
NM_001322421.1:c.*63G>C
|
NP_001309350.1:n.*63G>C
|
|
NM_001322422.1:c.*63G>C
|
NP_001309351.1:n.*63G>C
|
|
NM_001362758.1:c.*223G>C
|
NP_001349687.1:n.*223G>C
|
|
NR_136327.1:n.893G>C
|
|
|
XM_005260619.3:c.*63G>C
|
XP_005260676.1:n.*63G>C
|
|
XM_017028135.1:c.932G>C
|
XP_016883624.1:p.Cys311Ser
|
|
XM_017028136.1:c.830G>C
|
XP_016883625.1:p.Cys277Ser
|
|
NM_001250.6:c.*63G>C
MANE Select
|
NP_001241.1:n.*63G>C
|
|
NM_001302753.2:c.*223G>C
|
NP_001289682.1:n.*223G>C
|
|
NM_001322421.2:c.*63G>C
|
NP_001309350.1:n.*63G>C
|
|
NM_001322422.2:c.*63G>C
|
NP_001309351.1:n.*63G>C
|
|
NM_001362758.2:c.*223G>C
|
NP_001349687.1:n.*223G>C
|
|
NM_152854.4:c.*223G>C
|
NP_690593.1:n.*223G>C
|
|
NR_126502.2:n.930G>C
|
|
|
NR_136327.2:n.833G>C
|
|
|