ENST00000356231.4:c.2104T>G
MANE Select
|
ENSP00000348564.3:p.Phe702Val
|
|
ENST00000643434.1:c.*1282T>G
|
ENSP00000494699.1:n.*1282T>G
|
|
ENST00000356231.3:c.2104T>G
|
ENSP00000348564.3:p.Phe702Val
|
|
ENST00000562465.5:c.97T>G
|
ENSP00000454246.1:p.Phe33Val
|
|
NM_138477.2:c.2104T>G
|
NP_612486.2:p.Phe702Val
|
|
XM_005254176.3:c.2107T>G
|
XP_005254233.1:p.Phe703Val
|
|
XM_011521270.1:c.2131T>G
|
XP_011519572.1:p.Phe711Val
|
|
XM_011521271.1:c.2128T>G
|
XP_011519573.1:p.Phe710Val
|
|
XM_011521272.1:c.2131T>G
|
XP_011519574.1:p.Phe711Val
|
|
XM_011521273.1:c.2131T>G
|
XP_011519575.1:p.Phe711Val
|
|
XM_011521274.1:c.1096T>G
|
XP_011519576.1:p.Phe366Val
|
|
XM_011521275.1:c.1348T>G
|
XP_011519577.1:p.Phe450Val
|
|
XR_931757.1:n.2104T>G
|
|
|
NM_138477.4:c.2104T>G
MANE Select
|
NP_612486.2:p.Phe702Val
|
|
XM_005254176.5:c.2107T>G
|
XP_005254233.1:p.Phe703Val
|
|
XM_011521270.2:c.2131T>G
|
XP_011519572.1:p.Phe711Val
|
|
XM_011521271.2:c.2128T>G
|
XP_011519573.1:p.Phe710Val
|
|
XM_011521274.2:c.1096T>G
|
XP_011519576.1:p.Phe366Val
|
|
XR_001751104.1:n.2161T>G
|
|
|
XR_001751105.1:n.2161T>G
|
|
|
XR_931757.2:n.2124T>G
|
|
|