ENST00000369538.4:c.519T=
|
ENSP00000358551.4:p.Asn173=
|
|
ENST00000520113.7:c.531T=
MANE Select
|
ENSP00000430075.3:p.Asn177=
|
|
ENST00000637080.1:c.534T=
|
ENSP00000489753.1:p.Asn178=
|
|
ENST00000639077.1:n.196T=
|
|
|
ENST00000369538.3:c.618T=
|
ENSP00000358551.3:p.Asn206=
|
|
ENST00000485564.3:n.405T=
|
|
|
ENST00000520113.6:c.630T=
|
ENSP00000430075.2:p.Asn210=
|
|
NM_000036.2:c.630T=
|
NP_000027.2:p.Asn210=
|
|
NM_001172626.1:c.618T=
|
NP_001166097.1:p.Asn206=
|
|
NM_000036.3:c.531T=
MANE Select
|
NP_000027.3:p.Asn177=
|
|
NM_001172626.2:c.519T=
|
NP_001166097.2:p.Asn173=
|
|