ENST00000369538.4:c.376G>T
|
ENSP00000358551.4:p.Val126Phe
|
|
ENST00000520113.7:c.388G>T
MANE Select
|
ENSP00000430075.3:p.Val130Phe
|
|
ENST00000637080.1:c.391G>T
|
ENSP00000489753.1:p.Val131Phe
|
|
ENST00000639077.1:n.53G>T
|
|
|
ENST00000369538.3:c.475G>T
|
ENSP00000358551.3:p.Val159Phe
|
|
ENST00000485564.3:n.262G>T
|
|
|
ENST00000520113.6:c.487G>T
|
ENSP00000430075.2:p.Val163Phe
|
|
NM_000036.2:c.487G>T
|
NP_000027.2:p.Val163Phe
|
|
NM_001172626.1:c.475G>T
|
NP_001166097.1:p.Val159Phe
|
|
NM_000036.3:c.388G>T
MANE Select
|
NP_000027.3:p.Val130Phe
|
|
NM_001172626.2:c.376G>T
|
NP_001166097.2:p.Val126Phe
|
|