ENST00000470050.2:c.1695A>T
|
ENSP00000515580.1:p.Glu565Asp
|
|
ENST00000703945.1:c.1611A>T
|
ENSP00000515578.1:p.Glu537Asp
|
|
ENST00000703946.1:c.1265+4362A>T
|
ENSP00000515579.1:n.1265+4362A>T
|
|
ENST00000703947.1:c.1305A>T
|
ENSP00000515581.1:p.Glu435Asp
|
|
ENST00000703948.1:c.*1312A>T
|
ENSP00000515582.1:n.*1312A>T
|
|
ENST00000703949.1:c.1695A>T
|
ENSP00000515583.1:p.Glu565Asp
|
|
ENST00000703950.1:c.1695A>T
|
ENSP00000515584.1:p.Glu565Asp
|
|
ENST00000703951.1:c.1265+4362A>T
|
ENSP00000515585.1:n.1265+4362A>T
|
|
ENST00000703952.1:c.1265+4362A>T
|
ENSP00000515586.1:n.1265+4362A>T
|
|
ENST00000703953.1:c.*958A>T
|
ENSP00000515587.1:n.*958A>T
|
|
ENST00000703954.1:c.1575A>T
|
ENSP00000515588.1:p.Glu525Asp
|
|
ENST00000703955.1:n.2245A>T
|
|
|
ENST00000703957.1:n.200A>T
|
|
|
ENST00000298649.8:c.1692A>T
|
ENSP00000298649.3:p.Glu564Asp
|
|
ENST00000359426.7:c.1695A>T
MANE Select
|
ENSP00000352398.6:p.Glu565Asp
|
|
ENST00000436817.6:c.1707A>T
|
ENSP00000415949.2:p.Glu569Asp
|
|
ENST00000493591.6:c.*1583A>T
|
ENSP00000494917.1:n.*1583A>T
|
|
ENST00000643399.2:c.1707A>T
MANE Plus Clinical
|
ENSP00000494664.1:p.Glu569Asp
|
|
ENST00000298649.7:c.1692A>T
|
ENSP00000298649.3:p.Glu564Asp
|
|
ENST00000359426.6:c.1695A>T
|
ENSP00000352398.6:p.Glu565Asp
|
|
ENST00000360289.6:c.1659A>T
|
ENSP00000353433.2:p.Glu553Asp
|
|
ENST00000448642.6:c.1707A>T
|
ENSP00000402103.3:p.Glu569Asp
|
|
ENST00000494253.1:n.1921A>T
|
|
|
NM_000188.2:c.1695A>T
|
NP_000179.2:p.Glu565Asp
|
|
NM_033496.2:c.1692A>T
|
NP_277031.1:p.Glu564Asp
|
|
NM_033497.2:c.1707A>T
|
NP_277032.1:p.Glu569Asp
|
|
NM_033498.2:c.1707A>T
|
NP_277033.1:p.Glu569Asp
|
|
NM_033500.2:c.1659A>T , LRG_365t1:c.1659A>T
|
NP_277035.2:p.Glu553Asp
|
|
XM_005269735.2:c.1824A>T
|
XP_005269792.1:p.Glu608Asp
|
|
XM_005269736.1:c.1707A>T
|
XP_005269793.1:p.Glu569Asp
|
|
XM_005269737.1:c.1611A>T
|
XP_005269794.1:p.Glu537Asp
|
|
XM_011539732.1:c.1659A>T
|
XP_011538034.1:p.Glu553Asp
|
|
XM_011539733.1:c.1653A>T
|
XP_011538035.1:p.Glu551Asp
|
|
XM_011539734.1:c.1650A>T
|
XP_011538036.1:p.Glu550Asp
|
|
NM_001322364.1:c.1707A>T
|
NP_001309293.1:p.Glu569Asp
|
|
NM_001322365.1:c.1800A>T
|
NP_001309294.1:p.Glu600Asp
|
|
NM_001322366.1:c.1611A>T
|
NP_001309295.1:p.Glu537Asp
|
|
NM_001322367.1:c.1599A>T
|
NP_001309296.1:p.Glu533Asp
|
|
NM_001358263.1:c.1707A>T
MANE Plus Clinical
|
NP_001345192.1:p.Glu569Asp
|
|
XM_024447969.1:c.1707A>T
|
XP_024303737.1:p.Glu569Asp
|
|
NM_000188.3:c.1695A>T
MANE Select
|
NP_000179.2:p.Glu565Asp
|
|
NM_001322364.2:c.1707A>T
|
NP_001309293.1:p.Glu569Asp
|
|
NM_001322365.2:c.1800A>T
|
NP_001309294.1:p.Glu600Asp
|
|
NM_033496.3:c.1692A>T
|
NP_277031.1:p.Glu564Asp
|
|
NM_033497.3:c.1707A>T
|
NP_277032.1:p.Glu569Asp
|
|
NM_033498.3:c.1707A>T
|
NP_277033.1:p.Glu569Asp
|
|