ENST00000496887.7:c.771+1724T=
|
ENSP00000434560.2:n.771+1724T=
|
|
ENST00000646564.2:c.588+1724T=
|
ENSP00000495806.2:n.588+1724T=
|
|
ENST00000155840.12:c.1090T=
MANE Select
|
ENSP00000155840.2:p.Phe364=
|
|
ENST00000335475.6:c.709T=
|
ENSP00000334497.5:p.Phe237=
|
|
ENST00000646564.1:c.234+1724T=
|
ENSP00000495806.1:n.234+1724T=
|
|
ENST00000155840.9:c.1090T=
|
ENSP00000155840.2:p.Phe364=
|
|
ENST00000335475.5:c.709T=
|
ENSP00000334497.5:p.Phe237=
|
|
NM_000218.2:c.1090T= , LRG_287t1:c.1090T=
|
NP_000209.2:p.Phe364=
|
|
NM_181798.1:c.709T= , LRG_287t2:c.709T=
|
NP_861463.1:p.Phe237=
|
|
NM_000218.3:c.1090T=
MANE Select
|
NP_000209.2:p.Phe364=
|
|