ENST00000682565.1:c.7681T>G
|
ENSP00000507671.1:p.Phe2561Val
|
|
ENST00000682801.1:c.7681T>G
|
ENSP00000507862.1:p.Phe2561Val
|
|
ENST00000682859.1:c.7681T>G
|
ENSP00000508222.1:p.Phe2561Val
|
|
ENST00000683791.1:c.1073T>G
|
|
|
ENST00000684460.1:c.5133T>G
|
|
|
ENST00000684548.1:c.7681T>G
|
ENSP00000507421.1:p.Phe2561Val
|
|
ENST00000684590.1:c.2128T>G
|
ENSP00000507376.1:p.Phe710Val
|
|
ENST00000684656.1:c.5133T>G
|
|
|
ENST00000613296.6:c.8062T>G
MANE Select
|
ENSP00000482968.1:p.Phe2688Val
|
|
ENST00000651434.1:c.896-29754T>G
|
|
|
ENST00000423048.5:c.2893T>G
|
ENSP00000399833.1:p.Phe965Val
|
|
ENST00000484298.5:c.7936T>G
|
ENSP00000478155.1:p.Phe2646Val
|
|
ENST00000613296.4:c.8062T>G
|
ENSP00000482968.1:p.Phe2688Val
|
|
ENST00000614410.4:c.8062T>G
|
ENSP00000479094.1:p.Phe2688Val
|
|
ENST00000620466.4:n.1865T>G
|
|
|
NM_015120.4:c.8065T>G , LRG_741t1:c.8065T>G
|
NP_055935.4:p.Phe2689Val
|
|
NM_001378454.1:c.8062T>G
MANE Select
|
NP_001365383.1:p.Phe2688Val
|
|