ENST00000344265.8:c.812T=
|
ENSP00000342931.3:p.Met271=
|
|
ENST00000350375.7:c.734T=
MANE Select
|
ENSP00000263781.2:p.Met245=
|
|
ENST00000344265.7:c.812T=
|
ENSP00000342931.3:p.Met271=
|
|
ENST00000350375.6:c.734T=
|
ENSP00000263781.2:p.Met245=
|
|
ENST00000560656.1:c.508T=
|
ENSP00000452610.1:p.Ter170=
|
|
ENST00000561167.5:c.509T=
|
ENSP00000454072.1:p.Met170=
|
|
NM_000306.3:c.734T=
|
NP_000297.1:p.Met245=
|
|
NM_001122757.2:c.812T=
|
NP_001116229.1:p.Met271=
|
|
NM_000306.4:c.734T=
MANE Select
|
NP_000297.1:p.Met245=
|
|
NM_001122757.3:c.812T=
|
NP_001116229.1:p.Met271=
|
|