|
NM_000081.4:c.8281A>T
MANE Select
|
NP_000072.2:p.Arg2761Ter
|
|
ENST00000389793.7:c.8281A>T
MANE Select
|
ENSP00000374443.2:p.Arg2761Ter
|
|
NM_000081.3:c.8281A>T , LRG_143t1:c.8281A>T
|
NP_000072.2:p.Arg2761Ter
|
|
NM_001301365.1:c.8281A>T , LRG_143t2:c.8281A>T
|
NP_001288294.1:p.Arg2761Ter
|
|
ENST00000389793.6:c.8281A>T
|
ENSP00000374443.2:p.Arg2761Ter
|
|
ENST00000389794.7:c.*3705A>T
|
ENSP00000374444.4:n.*3705A>T
|
|
ENST00000461526.1:n.184A>T
|
|
|
ENST00000461526.2:c.2956A>T
|
ENSP00000513165.1:p.Arg986Ter
|
|
ENST00000475277.2:c.376A>T
|
ENSP00000513164.1:p.Arg126Ter
|
|
ENST00000697178.1:c.*3705A>T
|
ENSP00000513163.1:n.*3705A>T
|
|
ENST00000697236.1:c.1990A>T
|
ENSP00000513203.1:p.Arg664Ter
|
|
ENST00000697240.1:c.415A>T
|
ENSP00000513205.1:p.Arg139Ter
|
|
ENST00000697241.1:c.2761A>T
|
ENSP00000513206.1:p.Arg921Ter
|
|
XM_011544031.1:c.8443A>T
|
XP_011542333.1:p.Arg2815Ter
|
|
XM_011544032.1:c.8443A>T
|
XP_011542334.1:p.Arg2815Ter
|
|
XM_011544033.1:c.8443A>T
|
XP_011542335.1:p.Arg2815Ter
|
|
XM_011544033.2:c.8443A>T
|
XP_011542335.1:p.Arg2815Ter
|
|
XM_011544034.1:c.8305A>T
|
XP_011542336.1:p.Arg2769Ter
|
|
XM_011544035.1:c.8443A>T
|
XP_011542337.1:p.Arg2815Ter
|
|
XM_011544035.2:c.8443A>T
|
XP_011542337.1:p.Arg2815Ter
|
|
XM_011544036.1:c.6106A>T
|
XP_011542338.1:p.Arg2036Ter
|
|
XM_011544036.2:c.6106A>T
|
XP_011542338.1:p.Arg2036Ter
|
|
XM_011544037.1:c.8443A>T
|
XP_011542339.1:p.Arg2815Ter
|
|
XM_011544037.2:c.8443A>T
|
XP_011542339.1:p.Arg2815Ter
|
|
XM_011544038.1:c.8443A>T
|
XP_011542340.1:p.Arg2815Ter
|
|
XM_017000150.1:c.8443A>T
|
XP_016855639.1:p.Arg2815Ter
|
|
XR_001736946.2:n.8625A>T
|
|
|
XR_001736947.1:n.8463A>T
|
|
|
XR_001736948.1:n.7912A>T
|
|