ENST00000369538.4:c.1337G>T
|
ENSP00000358551.4:p.Cys446Phe
|
|
ENST00000520113.7:c.1349G>T
MANE Select
|
ENSP00000430075.3:p.Cys450Phe
|
|
ENST00000637080.1:c.1132G>T
|
ENSP00000489753.1:n.1132G>T
|
|
ENST00000639077.1:n.1014G>T
|
|
|
ENST00000369538.3:c.1436G>T
|
ENSP00000358551.3:p.Cys479Phe
|
|
ENST00000520113.6:c.1448G>T
|
ENSP00000430075.2:p.Cys483Phe
|
|
NM_000036.2:c.1448G>T
|
NP_000027.2:p.Cys483Phe
|
|
NM_001172626.1:c.1436G>T
|
NP_001166097.1:p.Cys479Phe
|
|
NM_000036.3:c.1349G>T
MANE Select
|
NP_000027.3:p.Cys450Phe
|
|
NM_001172626.2:c.1337G>T
|
NP_001166097.2:p.Cys446Phe
|
|