ENST00000496887.7:c.718A=
|
ENSP00000434560.2:p.Thr240=
|
|
ENST00000646564.2:c.535A=
|
ENSP00000495806.2:p.Thr179=
|
|
ENST00000155840.12:c.979A=
MANE Select
|
ENSP00000155840.2:p.Thr327=
|
|
ENST00000335475.6:c.598A=
|
ENSP00000334497.5:p.Thr200=
|
|
ENST00000646564.1:c.181A=
|
ENSP00000495806.1:p.Thr61=
|
|
ENST00000155840.9:c.979A=
|
ENSP00000155840.2:p.Thr327=
|
|
ENST00000335475.5:c.598A=
|
ENSP00000334497.5:p.Thr200=
|
|
NM_000218.2:c.979A= , LRG_287t1:c.979A=
|
NP_000209.2:p.Thr327=
|
|
NM_181798.1:c.598A= , LRG_287t2:c.598A=
|
NP_861463.1:p.Thr200=
|
|
NM_000218.3:c.979A=
MANE Select
|
NP_000209.2:p.Thr327=
|
|