ENST00000369538.4:c.1207A>G
|
ENSP00000358551.4:p.Ile403Val
|
|
ENST00000520113.7:c.1219A>G
MANE Select
|
ENSP00000430075.3:p.Ile407Val
|
|
ENST00000637080.1:c.1002A>G
|
ENSP00000489753.1:n.1002A>G
|
|
ENST00000639077.1:n.884A>G
|
|
|
ENST00000369538.3:c.1306A>G
|
ENSP00000358551.3:p.Ile436Val
|
|
ENST00000520113.6:c.1318A>G
|
ENSP00000430075.2:p.Ile440Val
|
|
NM_000036.2:c.1318A>G
|
NP_000027.2:p.Ile440Val
|
|
NM_001172626.1:c.1306A>G
|
NP_001166097.1:p.Ile436Val
|
|
NM_000036.3:c.1219A>G
MANE Select
|
NP_000027.3:p.Ile407Val
|
|
NM_001172626.2:c.1207A>G
|
NP_001166097.2:p.Ile403Val
|
|