ENST00000489304.6:c.983G>C
|
ENSP00000512096.1:n.983G>C
|
|
ENST00000695675.1:n.2776G>C
|
|
|
ENST00000372285.8:c.*66G>C
MANE Select
|
ENSP00000361359.3:n.*66G>C
|
|
ENST00000372276.7:c.*226G>C
|
ENSP00000361350.3:n.*226G>C
|
|
ENST00000372285.7:c.*66G>C
|
ENSP00000361359.3:n.*66G>C
|
|
ENST00000466205.5:c.802G>C
|
|
|
ENST00000489304.5:n.976G>C
|
|
|
ENST00000620709.4:c.*447G>C
|
ENSP00000484074.1:n.*447G>C
|
|
NM_001250.5:c.*66G>C
|
NP_001241.1:n.*66G>C
|
|
NM_001302753.1:c.*226G>C
|
NP_001289682.1:n.*226G>C
|
|
NM_152854.3:c.*226G>C
|
NP_690593.1:n.*226G>C
|
|
NR_126502.1:n.993G>C
|
|
|
XM_005260617.2:c.*66G>C
|
XP_005260674.1:n.*66G>C
|
|
XM_005260619.2:c.*66G>C
|
XP_005260676.1:n.*66G>C
|
|
NM_001322421.1:c.*66G>C
|
NP_001309350.1:n.*66G>C
|
|
NM_001322422.1:c.*66G>C
|
NP_001309351.1:n.*66G>C
|
|
NM_001362758.1:c.*226G>C
|
NP_001349687.1:n.*226G>C
|
|
NR_136327.1:n.896G>C
|
|
|
XM_005260619.3:c.*66G>C
|
XP_005260676.1:n.*66G>C
|
|
XM_017028135.1:c.935G>C
|
XP_016883624.1:p.Cys312Ser
|
|
XM_017028136.1:c.833G>C
|
XP_016883625.1:p.Cys278Ser
|
|
NM_001250.6:c.*66G>C
MANE Select
|
NP_001241.1:n.*66G>C
|
|
NM_001302753.2:c.*226G>C
|
NP_001289682.1:n.*226G>C
|
|
NM_001322421.2:c.*66G>C
|
NP_001309350.1:n.*66G>C
|
|
NM_001322422.2:c.*66G>C
|
NP_001309351.1:n.*66G>C
|
|
NM_001362758.2:c.*226G>C
|
NP_001349687.1:n.*226G>C
|
|
NM_152854.4:c.*226G>C
|
NP_690593.1:n.*226G>C
|
|
NR_126502.2:n.933G>C
|
|
|
NR_136327.2:n.836G>C
|
|
|