ENST00000496887.7:c.1009T=
|
ENSP00000434560.2:p.Phe337=
|
|
ENST00000646564.2:c.826T=
|
ENSP00000495806.2:p.Phe276=
|
|
ENST00000155840.12:c.1366T=
MANE Select
|
ENSP00000155840.2:p.Phe456=
|
|
ENST00000335475.6:c.985T=
|
ENSP00000334497.5:p.Phe329=
|
|
ENST00000646564.1:c.472T=
|
ENSP00000495806.1:p.Phe158=
|
|
ENST00000155840.9:c.1366T=
|
ENSP00000155840.2:p.Phe456=
|
|
ENST00000335475.5:c.985T=
|
ENSP00000334497.5:p.Phe329=
|
|
NM_000218.2:c.1366T= , LRG_287t1:c.1366T=
|
NP_000209.2:p.Phe456=
|
|
NM_181798.1:c.985T= , LRG_287t2:c.985T=
|
NP_861463.1:p.Phe329=
|
|
NM_000218.3:c.1366T=
MANE Select
|
NP_000209.2:p.Phe456=
|
|