ENST00000496887.7:c.654G=
|
ENSP00000434560.2:p.Trp218=
|
|
ENST00000646564.2:c.478-10455G=
|
ENSP00000495806.2:n.478-10455G=
|
|
ENST00000155840.12:c.915G=
MANE Select
|
ENSP00000155840.2:p.Trp305=
|
|
ENST00000335475.6:c.534G=
|
ENSP00000334497.5:p.Trp178=
|
|
ENST00000646564.1:c.124-10455G=
|
ENSP00000495806.1:n.124-10455G=
|
|
ENST00000155840.9:c.915G=
|
ENSP00000155840.2:p.Trp305=
|
|
ENST00000335475.5:c.534G=
|
ENSP00000334497.5:p.Trp178=
|
|
NM_000218.2:c.915G= , LRG_287t1:c.915G=
|
NP_000209.2:p.Trp305=
|
|
NM_181798.1:c.534G= , LRG_287t2:c.534G=
|
NP_861463.1:p.Trp178=
|
|
NM_000218.3:c.915G=
MANE Select
|
NP_000209.2:p.Trp305=
|
|