ENST00000369538.4:c.526T=
|
ENSP00000358551.4:p.Phe176=
|
|
ENST00000520113.7:c.538T=
MANE Select
|
ENSP00000430075.3:p.Phe180=
|
|
ENST00000637080.1:c.541T=
|
ENSP00000489753.1:p.Phe181=
|
|
ENST00000639077.1:n.203T=
|
|
|
ENST00000369538.3:c.625T=
|
ENSP00000358551.3:p.Phe209=
|
|
ENST00000485564.3:n.412T=
|
|
|
ENST00000520113.6:c.637T=
|
ENSP00000430075.2:p.Phe213=
|
|
NM_000036.2:c.637T=
|
NP_000027.2:p.Phe213=
|
|
NM_001172626.1:c.625T=
|
NP_001166097.1:p.Phe209=
|
|
NM_000036.3:c.538T=
MANE Select
|
NP_000027.3:p.Phe180=
|
|
NM_001172626.2:c.526T=
|
NP_001166097.2:p.Phe176=
|
|