ENST00000369538.4:c.510G=
|
ENSP00000358551.4:p.Trp170=
|
|
ENST00000520113.7:c.522G=
MANE Select
|
ENSP00000430075.3:p.Trp174=
|
|
ENST00000637080.1:c.525G=
|
ENSP00000489753.1:p.Trp175=
|
|
ENST00000639077.1:n.187G=
|
|
|
ENST00000369538.3:c.609G=
|
ENSP00000358551.3:p.Trp203=
|
|
ENST00000485564.3:n.396G=
|
|
|
ENST00000520113.6:c.621G=
|
ENSP00000430075.2:p.Trp207=
|
|
NM_000036.2:c.621G=
|
NP_000027.2:p.Trp207=
|
|
NM_001172626.1:c.609G=
|
NP_001166097.1:p.Trp203=
|
|
NM_000036.3:c.522G=
MANE Select
|
NP_000027.3:p.Trp174=
|
|
NM_001172626.2:c.510G=
|
NP_001166097.2:p.Trp170=
|
|