ENST00000369538.4:c.1319T>C
|
ENSP00000358551.4:p.Val440Ala
|
|
ENST00000520113.7:c.1331T>C
MANE Select
|
ENSP00000430075.3:p.Val444Ala
|
|
ENST00000637080.1:c.1114T>C
|
ENSP00000489753.1:n.1114T>C
|
|
ENST00000639077.1:n.996T>C
|
|
|
ENST00000369538.3:c.1418T>C
|
ENSP00000358551.3:p.Val473Ala
|
|
ENST00000520113.6:c.1430T>C
|
ENSP00000430075.2:p.Val477Ala
|
|
NM_000036.2:c.1430T>C
|
NP_000027.2:p.Val477Ala
|
|
NM_001172626.1:c.1418T>C
|
NP_001166097.1:p.Val473Ala
|
|
NM_000036.3:c.1331T>C
MANE Select
|
NP_000027.3:p.Val444Ala
|
|
NM_001172626.2:c.1319T>C
|
NP_001166097.2:p.Val440Ala
|
|