ENST00000470050.2:c.1400A>G
|
ENSP00000515580.1:p.His467Arg
|
|
ENST00000703945.1:c.1316A>G
|
ENSP00000515578.1:p.His439Arg
|
|
ENST00000703946.1:c.1265+2526A>G
|
ENSP00000515579.1:n.1265+2526A>G
|
|
ENST00000703947.1:c.1010A>G
|
ENSP00000515581.1:p.His337Arg
|
|
ENST00000703948.1:c.*1017A>G
|
ENSP00000515582.1:n.*1017A>G
|
|
ENST00000703949.1:c.1400A>G
|
ENSP00000515583.1:p.His467Arg
|
|
ENST00000703950.1:c.1400A>G
|
ENSP00000515584.1:p.His467Arg
|
|
ENST00000703951.1:c.1265+2526A>G
|
ENSP00000515585.1:n.1265+2526A>G
|
|
ENST00000703952.1:c.1265+2526A>G
|
ENSP00000515586.1:n.1265+2526A>G
|
|
ENST00000703953.1:c.*663A>G
|
ENSP00000515587.1:n.*663A>G
|
|
ENST00000703954.1:c.1280A>G
|
ENSP00000515588.1:p.His427Arg
|
|
ENST00000703955.1:n.1950A>G
|
|
|
ENST00000298649.8:c.1397A>G
|
ENSP00000298649.3:p.His466Arg
|
|
ENST00000359426.7:c.1400A>G
MANE Select
|
ENSP00000352398.6:p.His467Arg
|
|
ENST00000436817.6:c.1412A>G
|
ENSP00000415949.2:p.His471Arg
|
|
ENST00000493591.6:c.*1288A>G
|
ENSP00000494917.1:n.*1288A>G
|
|
ENST00000643399.2:c.1412A>G
MANE Plus Clinical
|
ENSP00000494664.1:p.His471Arg
|
|
ENST00000298649.7:c.1397A>G
|
ENSP00000298649.3:p.His466Arg
|
|
ENST00000359426.6:c.1400A>G
|
ENSP00000352398.6:p.His467Arg
|
|
ENST00000360289.6:c.1364A>G
|
ENSP00000353433.2:p.His455Arg
|
|
ENST00000448642.6:c.1412A>G
|
ENSP00000402103.3:p.His471Arg
|
|
ENST00000494253.1:n.1626A>G
|
|
|
NM_000188.2:c.1400A>G
|
NP_000179.2:p.His467Arg
|
|
NM_033496.2:c.1397A>G
|
NP_277031.1:p.His466Arg
|
|
NM_033497.2:c.1412A>G
|
NP_277032.1:p.His471Arg
|
|
NM_033498.2:c.1412A>G
|
NP_277033.1:p.His471Arg
|
|
NM_033500.2:c.1364A>G , LRG_365t1:c.1364A>G
|
NP_277035.2:p.His455Arg
|
|
XM_005269735.2:c.1529A>G
|
XP_005269792.1:p.His510Arg
|
|
XM_005269736.1:c.1412A>G
|
XP_005269793.1:p.His471Arg
|
|
XM_005269737.1:c.1316A>G
|
XP_005269794.1:p.His439Arg
|
|
XM_011539732.1:c.1364A>G
|
XP_011538034.1:p.His455Arg
|
|
XM_011539733.1:c.1358A>G
|
XP_011538035.1:p.His453Arg
|
|
XM_011539734.1:c.1355A>G
|
XP_011538036.1:p.His452Arg
|
|
NM_001322364.1:c.1412A>G
|
NP_001309293.1:p.His471Arg
|
|
NM_001322365.1:c.1505A>G
|
NP_001309294.1:p.His502Arg
|
|
NM_001322366.1:c.1316A>G
|
NP_001309295.1:p.His439Arg
|
|
NM_001322367.1:c.1304A>G
|
NP_001309296.1:p.His435Arg
|
|
NM_001358263.1:c.1412A>G
MANE Plus Clinical
|
NP_001345192.1:p.His471Arg
|
|
XM_024447969.1:c.1412A>G
|
XP_024303737.1:p.His471Arg
|
|
NM_000188.3:c.1400A>G
MANE Select
|
NP_000179.2:p.His467Arg
|
|
NM_001322364.2:c.1412A>G
|
NP_001309293.1:p.His471Arg
|
|
NM_001322365.2:c.1505A>G
|
NP_001309294.1:p.His502Arg
|
|
NM_033496.3:c.1397A>G
|
NP_277031.1:p.His466Arg
|
|
NM_033497.3:c.1412A>G
|
NP_277032.1:p.His471Arg
|
|
NM_033498.3:c.1412A>G
|
NP_277033.1:p.His471Arg
|
|