ENST00000470050.2:c.1338G>T
|
ENSP00000515580.1:p.Glu446Asp
|
|
ENST00000703945.1:c.1254G>T
|
ENSP00000515578.1:p.Glu418Asp
|
|
ENST00000703946.1:c.1265+2464G>T
|
ENSP00000515579.1:n.1265+2464G>T
|
|
ENST00000703947.1:c.948G>T
|
ENSP00000515581.1:p.Glu316Asp
|
|
ENST00000703948.1:c.*955G>T
|
ENSP00000515582.1:n.*955G>T
|
|
ENST00000703949.1:c.1338G>T
|
ENSP00000515583.1:p.Glu446Asp
|
|
ENST00000703950.1:c.1338G>T
|
ENSP00000515584.1:p.Glu446Asp
|
|
ENST00000703951.1:c.1265+2464G>T
|
ENSP00000515585.1:n.1265+2464G>T
|
|
ENST00000703952.1:c.1265+2464G>T
|
ENSP00000515586.1:n.1265+2464G>T
|
|
ENST00000703953.1:c.*601G>T
|
ENSP00000515587.1:n.*601G>T
|
|
ENST00000703954.1:c.1218G>T
|
ENSP00000515588.1:p.Glu406Asp
|
|
ENST00000703955.1:n.1888G>T
|
|
|
ENST00000298649.8:c.1335G>T
|
ENSP00000298649.3:p.Glu445Asp
|
|
ENST00000359426.7:c.1338G>T
MANE Select
|
ENSP00000352398.6:p.Glu446Asp
|
|
ENST00000436817.6:c.1350G>T
|
ENSP00000415949.2:p.Glu450Asp
|
|
ENST00000493591.6:c.*1226G>T
|
ENSP00000494917.1:n.*1226G>T
|
|
ENST00000643399.2:c.1350G>T
MANE Plus Clinical
|
ENSP00000494664.1:p.Glu450Asp
|
|
ENST00000298649.7:c.1335G>T
|
ENSP00000298649.3:p.Glu445Asp
|
|
ENST00000359426.6:c.1338G>T
|
ENSP00000352398.6:p.Glu446Asp
|
|
ENST00000360289.6:c.1302G>T
|
ENSP00000353433.2:p.Glu434Asp
|
|
ENST00000448642.6:c.1350G>T
|
ENSP00000402103.3:p.Glu450Asp
|
|
ENST00000494253.1:n.1564G>T
|
|
|
NM_000188.2:c.1338G>T
|
NP_000179.2:p.Glu446Asp
|
|
NM_033496.2:c.1335G>T
|
NP_277031.1:p.Glu445Asp
|
|
NM_033497.2:c.1350G>T
|
NP_277032.1:p.Glu450Asp
|
|
NM_033498.2:c.1350G>T
|
NP_277033.1:p.Glu450Asp
|
|
NM_033500.2:c.1302G>T , LRG_365t1:c.1302G>T
|
NP_277035.2:p.Glu434Asp
|
|
XM_005269735.2:c.1467G>T
|
XP_005269792.1:p.Glu489Asp
|
|
XM_005269736.1:c.1350G>T
|
XP_005269793.1:p.Glu450Asp
|
|
XM_005269737.1:c.1254G>T
|
XP_005269794.1:p.Glu418Asp
|
|
XM_011539732.1:c.1302G>T
|
XP_011538034.1:p.Glu434Asp
|
|
XM_011539733.1:c.1296G>T
|
XP_011538035.1:p.Glu432Asp
|
|
XM_011539734.1:c.1293G>T
|
XP_011538036.1:p.Glu431Asp
|
|
NM_001322364.1:c.1350G>T
|
NP_001309293.1:p.Glu450Asp
|
|
NM_001322365.1:c.1443G>T
|
NP_001309294.1:p.Glu481Asp
|
|
NM_001322366.1:c.1254G>T
|
NP_001309295.1:p.Glu418Asp
|
|
NM_001322367.1:c.1242G>T
|
NP_001309296.1:p.Glu414Asp
|
|
NM_001358263.1:c.1350G>T
MANE Plus Clinical
|
NP_001345192.1:p.Glu450Asp
|
|
XM_024447969.1:c.1350G>T
|
XP_024303737.1:p.Glu450Asp
|
|
NM_000188.3:c.1338G>T
MANE Select
|
NP_000179.2:p.Glu446Asp
|
|
NM_001322364.2:c.1350G>T
|
NP_001309293.1:p.Glu450Asp
|
|
NM_001322365.2:c.1443G>T
|
NP_001309294.1:p.Glu481Asp
|
|
NM_033496.3:c.1335G>T
|
NP_277031.1:p.Glu445Asp
|
|
NM_033497.3:c.1350G>T
|
NP_277032.1:p.Glu450Asp
|
|
NM_033498.3:c.1350G>T
|
NP_277033.1:p.Glu450Asp
|
|