ENST00000375128.5:c.781T=
MANE Select
|
ENSP00000364270.5:p.Cys261=
|
|
ENST00000375128.4:c.781T=
|
ENSP00000364270.4:p.Cys261=
|
|
ENST00000462523.5:c.*217T=
|
ENSP00000433006.1:n.*217T=
|
|
ENST00000485042.1:n.293T=
|
|
|
NM_000380.3:c.781T= , LRG_471t1:c.781T=
|
NP_000371.1:p.Cys261=
|
|
NR_027302.1:n.1129T=
|
|
|
XM_006717278.1:c.772+9T=
|
XP_006717341.1:n.772+9T=
|
|
XM_011518988.1:c.772+9T=
|
XP_011517290.1:n.772+9T=
|
|
NM_001354975.1:c.655T=
|
NP_001341904.1:p.Cys219=
|
|
NR_149091.1:n.626T=
|
|
|
NR_149092.1:n.792T=
|
|
|
NR_149093.1:n.1318T=
|
|
|
NR_149094.1:n.1212T=
|
|
|
NM_000380.4:c.781T=
MANE Select
|
NP_000371.1:p.Cys261=
|
|
NM_001354975.2:c.655T=
|
NP_001341904.1:p.Cys219=
|
|
NR_027302.2:n.1060T=
|
|
|
NR_149091.2:n.557T=
|
|
|
NR_149092.2:n.723T=
|
|
|
NR_149093.2:n.1249T=
|
|
|
NR_149094.2:n.1143T=
|
|
|