ENST00000369538.4:c.1325A>C
|
ENSP00000358551.4:p.Asn442Thr
|
|
ENST00000520113.7:c.1337A>C
MANE Select
|
ENSP00000430075.3:p.Asn446Thr
|
|
ENST00000637080.1:c.1120A>C
|
ENSP00000489753.1:n.1120A>C
|
|
ENST00000639077.1:n.1002A>C
|
|
|
ENST00000369538.3:c.1424A>C
|
ENSP00000358551.3:p.Asn475Thr
|
|
ENST00000520113.6:c.1436A>C
|
ENSP00000430075.2:p.Asn479Thr
|
|
NM_000036.2:c.1436A>C
|
NP_000027.2:p.Asn479Thr
|
|
NM_001172626.1:c.1424A>C
|
NP_001166097.1:p.Asn475Thr
|
|
NM_000036.3:c.1337A>C
MANE Select
|
NP_000027.3:p.Asn446Thr
|
|
NM_001172626.2:c.1325A>C
|
NP_001166097.2:p.Asn442Thr
|
|