ENST00000369538.4:c.385T>G
|
ENSP00000358551.4:p.Phe129Val
|
|
ENST00000520113.7:c.397T>G
MANE Select
|
ENSP00000430075.3:p.Phe133Val
|
|
ENST00000637080.1:c.400T>G
|
ENSP00000489753.1:p.Phe134Val
|
|
ENST00000639077.1:n.62T>G
|
|
|
ENST00000369538.3:c.484T>G
|
ENSP00000358551.3:p.Phe162Val
|
|
ENST00000485564.3:n.271T>G
|
|
|
ENST00000520113.6:c.496T>G
|
ENSP00000430075.2:p.Phe166Val
|
|
NM_000036.2:c.496T>G
|
NP_000027.2:p.Phe166Val
|
|
NM_001172626.1:c.484T>G
|
NP_001166097.1:p.Phe162Val
|
|
NM_000036.3:c.397T>G
MANE Select
|
NP_000027.3:p.Phe133Val
|
|
NM_001172626.2:c.385T>G
|
NP_001166097.2:p.Phe129Val
|
|