ENST00000496887.7:c.544G=
|
ENSP00000434560.2:p.Gly182=
|
|
ENST00000646564.2:c.478-10565G=
|
ENSP00000495806.2:n.478-10565G=
|
|
ENST00000155840.12:c.805G=
MANE Select
|
ENSP00000155840.2:p.Gly269=
|
|
ENST00000335475.6:c.424G=
|
ENSP00000334497.5:p.Gly142=
|
|
ENST00000646564.1:c.124-10565G=
|
ENSP00000495806.1:n.124-10565G=
|
|
ENST00000155840.9:c.805G=
|
ENSP00000155840.2:p.Gly269=
|
|
ENST00000335475.5:c.424G=
|
ENSP00000334497.5:p.Gly142=
|
|
ENST00000496887.6:c.544G=
|
ENSP00000434560.1:p.Gly182=
|
|
NM_000218.2:c.805G= , LRG_287t1:c.805G=
|
NP_000209.2:p.Gly269=
|
|
NM_181798.1:c.424G= , LRG_287t2:c.424G=
|
NP_861463.1:p.Gly142=
|
|
NM_000218.3:c.805G=
MANE Select
|
NP_000209.2:p.Gly269=
|
|