|
ENST00000317716.14:c.1579G=
MANE Select
|
ENSP00000325954.9:p.Val527=
|
|
|
ENST00000317716.13:c.1579G=
|
ENSP00000325954.9:p.Val527=
|
|
|
ENST00000466045.1:c.700+1973G=
|
ENSP00000419017.1:n.700+1973G=
|
|
|
ENST00000468477.1:c.60-2375G=
|
|
|
|
ENST00000470188.5:n.1849+1973G=
|
|
|
|
ENST00000478080.5:c.1315G=
|
ENSP00000417771.1:p.Val439=
|
|
|
NM_001301161.1:c.1315G=
|
NP_001288090.1:p.Val439=
|
|
|
NM_152750.4:c.1579G=
|
NP_689963.2:p.Val527=
|
|
|
XM_005250224.3:c.1315G=
|
XP_005250281.1:p.Val439=
|
|
|
XM_005250225.1:c.1579G=
|
XP_005250282.1:p.Val527=
|
|
|
XM_005250226.1:c.523G=
|
XP_005250283.1:p.Val175=
|
|
|
XM_006715905.1:c.1426+1973G=
|
XP_006715968.1:n.1426+1973G=
|
|
|
XM_006715906.2:c.1033G=
|
XP_006715969.1:p.Val345=
|
|
|
XM_011515955.1:c.1579G=
|
XP_011514257.1:p.Val527=
|
|
|
XM_011515956.1:c.1033G=
|
XP_011514258.1:p.Val345=
|
|
|
XM_011515957.1:c.1579G=
|
XP_011514259.1:p.Val527=
|
|
|
XM_011515958.1:c.1426+1973G=
|
XP_011514260.1:n.1426+1973G=
|
|
|
XM_011515959.1:c.523G=
|
XP_011514261.1:p.Val175=
|
|
|
XR_927414.1:n.1655G=
|
|
|
|
XM_005250224.5:c.1315G=
|
XP_005250281.1:p.Val439=
|
|
|
XM_005250225.2:c.1579G=
|
XP_005250282.1:p.Val527=
|
|
|
XM_006715905.2:c.1426+1973G=
|
XP_006715968.1:n.1426+1973G=
|
|
|
XM_011515955.2:c.1579G=
|
XP_011514257.1:p.Val527=
|
|
|
XM_011515956.2:c.1033G=
|
XP_011514258.1:p.Val345=
|
|
|
XM_011515957.2:c.1579G=
|
XP_011514259.1:p.Val527=
|
|
|
XM_011515958.2:c.1426+1973G=
|
XP_011514260.1:n.1426+1973G=
|
|
|
XM_011515959.2:c.523G=
|
XP_011514261.1:p.Val175=
|
|
|
XM_017011862.1:c.1579G=
|
XP_016867351.1:p.Val527=
|
|
|
XM_017011863.2:c.1033G=
|
XP_016867352.1:p.Val345=
|
|
|
XM_017011864.1:c.1033G=
|
XP_016867353.1:p.Val345=
|
|
|
XM_017011865.2:c.1162+1973G=
|
XP_016867354.1:n.1162+1973G=
|
|
|
XM_017011866.2:c.730G=
|
XP_016867355.1:p.Val244=
|
|
|
XM_017011867.2:c.880+1973G=
|
XP_016867356.1:n.880+1973G=
|
|
|
XM_024446689.1:c.523G=
|
XP_024302457.1:p.Val175=
|
|
|
XM_024446690.1:c.577+1973G=
|
XP_024302458.1:n.577+1973G=
|
|
|
XR_001744598.1:n.1655G=
|
|
|
|
XR_001744600.2:n.1655G=
|
|
|
|
XR_001744601.2:n.1655G=
|
|
|
|
XR_001744602.1:n.1672G=
|
|
|
|
XR_001744603.2:n.1672G=
|
|
|
|
XR_001744604.2:n.1502+1973G=
|
|
|
|
XR_001744605.2:n.1502+1973G=
|
|
|
|
XR_001744606.2:n.1502+1973G=
|
|
|
|
XR_001744607.2:n.1502+1973G=
|
|
|
|
XR_927414.2:n.1655G=
|
|
|
|
NM_152750.5:c.1579G=
MANE Select
|
NP_689963.2:p.Val527=
|
|
|
NM_001301161.2:c.1315G=
|
NP_001288090.1:p.Val439=
|
|
