ENST00000470094.2:c.9291T=
|
ENSP00000434898.2:p.Cys3097=
|
|
ENST00000528762.2:c.*658T=
|
ENSP00000433168.2:n.*658T=
|
|
ENST00000530893.7:c.8922T=
|
ENSP00000499438.2:p.Cys2974=
|
|
ENST00000665585.2:c.*853T=
|
ENSP00000499570.2:n.*853T=
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|
ENST00000666593.2:c.*136T=
|
ENSP00000499256.2:n.*136T=
|
|
ENST00000700202.2:c.9240T=
|
ENSP00000514856.2:p.Cys3080=
|
|
ENST00000700202.1:c.1707T=
|
ENSP00000514856.1:p.Cys569=
|
|
ENST00000700203.1:n.1418T=
|
|
|
ENST00000380152.8:c.9291T=
MANE Select
|
ENSP00000369497.3:p.Cys3097=
|
|
ENST00000544455.6:c.9291T=
|
ENSP00000439902.1:p.Cys3097=
|
|
ENST00000614259.2:c.9299T=
|
ENSP00000506251.1:n.9299T=
|
|
ENST00000665585.1:c.2169T=
|
|
|
ENST00000666593.1:c.313T=
|
ENSP00000499256.1:n.313T=
|
|
ENST00000680887.1:c.9291T=
|
ENSP00000505508.1:p.Cys3097=
|
|
ENST00000380152.7:c.9291T=
|
ENSP00000369497.3:p.Cys3097=
|
|
ENST00000470094.1:c.248T=
|
|
|
ENST00000544455.5:c.9291T=
|
ENSP00000439902.1:p.Cys3097=
|
|
NM_000059.3:c.9291T= , LRG_293t1:c.9291T=
|
NP_000050.2:p.Cys3097=
|
|
XM_011535203.1:c.9291T=
|
XP_011533505.1:p.Cys3097=
|
|
XM_011535204.1:c.9195T=
|
XP_011533506.1:p.Cys3065=
|
|
NM_000059.4:c.9291T=
MANE Select
|
NP_000050.3:p.Cys3097=
|
|