ENST00000476680.2:c.318-4283T>A
|
|
|
ENST00000537320.6:c.3215-4283T>A
|
ENSP00000443478.1:n.3215-4283T>A
|
|
ENST00000542877.6:c.3822T>A
|
ENSP00000442242.1:p.Arg1274=
|
|
ENST00000705190.1:c.1854T>A
|
ENSP00000516083.1:p.Arg618=
|
|
ENST00000705191.1:c.510T>A
|
ENSP00000516084.1:p.Arg170=
|
|
ENST00000705192.1:c.3869T>A
|
|
|
ENST00000350763.9:c.4911T>A
MANE Select
|
ENSP00000265131.4:p.Arg1637=
|
|
ENST00000341037.8:c.4365T>A
|
ENSP00000339553.4:p.Arg1455=
|
|
ENST00000350763.8:c.4911T>A
|
ENSP00000265131.4:p.Arg1637=
|
|
ENST00000423613.6:c.4307-4283T>A
|
ENSP00000411406.2:n.4307-4283T>A
|
|
ENST00000473855.1:n.229T>A
|
|
|
ENST00000476680.1:n.253-4283T>A
|
|
|
ENST00000498724.5:n.40-4283T>A
|
|
|
ENST00000535648.5:c.3822T>A
|
ENSP00000438152.2:p.Arg1274=
|
|
ENST00000537320.5:c.3215-4283T>A
|
ENSP00000443478.1:n.3215-4283T>A
|
|
ENST00000542877.5:c.3822T>A
|
ENSP00000442242.1:p.Arg1274=
|
|
ENST00000544972.1:c.598T>A
|
|
|
ENST00000635336.1:c.69T>A
|
ENSP00000489385.1:p.Arg23=
|
|
NM_002160.3:c.4911T>A
|
NP_002151.2:p.Arg1637=
|
|
XM_005251972.2:c.4638T>A
|
XP_005252029.1:p.Arg1546=
|
|
XM_005251973.2:c.4034-4283T>A
|
XP_005252030.1:n.4034-4283T>A
|
|
XM_005251974.2:c.3273T>A
|
XP_005252031.1:p.Arg1091=
|
|
XM_005251975.2:c.3215-4283T>A
|
XP_005252032.1:n.3215-4283T>A
|
|
XM_006717096.2:c.5187T>A
|
XP_006717159.1:p.Arg1729=
|
|
XM_006717097.2:c.4638T>A
|
XP_006717160.1:p.Arg1546=
|
|
XM_006717098.2:c.4365T>A
|
XP_006717161.1:p.Arg1455=
|
|
XM_006717100.2:c.4307-4283T>A
|
XP_006717163.1:n.4307-4283T>A
|
|
XM_006717101.2:c.3488-4283T>A
|
XP_006717164.1:n.3488-4283T>A
|
|
XM_011518622.1:c.4914T>A
|
XP_011516924.1:p.Arg1638=
|
|
XM_011518623.1:c.4914T>A
|
XP_011516925.1:p.Arg1638=
|
|
XM_011518624.1:c.4368T>A
|
XP_011516926.1:p.Arg1456=
|
|
XM_011518625.1:c.4580-4283T>A
|
XP_011516927.1:n.4580-4283T>A
|
|
XM_011518626.1:c.4095T>A
|
XP_011516928.1:p.Arg1365=
|
|
XM_011518627.1:c.3822T>A
|
XP_011516929.1:p.Arg1274=
|
|
XM_011518628.1:c.3761-4283T>A
|
XP_011516930.1:n.3761-4283T>A
|
|
XM_011518629.1:c.3546T>A
|
XP_011516931.1:p.Arg1182=
|
|
XM_005251972.4:c.4638T>A
|
XP_005252029.1:p.Arg1546=
|
|
XM_005251973.4:c.4034-4283T>A
|
XP_005252030.1:n.4034-4283T>A
|
|
XM_005251974.4:c.3273T>A
|
XP_005252031.1:p.Arg1091=
|
|
XM_005251975.4:c.3215-4283T>A
|
XP_005252032.1:n.3215-4283T>A
|
|
XM_006717096.4:c.5187T>A
|
XP_006717159.1:p.Arg1729=
|
|
XM_006717097.4:c.4638T>A
|
XP_006717160.1:p.Arg1546=
|
|
XM_006717098.4:c.4365T>A
|
XP_006717161.1:p.Arg1455=
|
|
XM_006717101.4:c.3488-4283T>A
|
XP_006717164.1:n.3488-4283T>A
|
|
XM_011518625.3:c.4580-4283T>A
|
XP_011516927.1:n.4580-4283T>A
|
|
XM_011518626.3:c.4095T>A
|
XP_011516928.1:p.Arg1365=
|
|
XM_011518628.3:c.3761-4283T>A
|
XP_011516930.1:n.3761-4283T>A
|
|
XM_011518629.3:c.3546T>A
|
XP_011516931.1:p.Arg1182=
|
|
XM_017014678.2:c.5460T>A
|
XP_016870167.1:p.Arg1820=
|
|
XM_017014679.2:c.5187T>A
|
XP_016870168.1:p.Arg1729=
|
|
XM_017014680.2:c.5184T>A
|
XP_016870169.1:p.Arg1728=
|
|
XM_017014681.2:c.4368T>A
|
XP_016870170.1:p.Arg1456=
|
|
XM_024447530.1:c.5460T>A
|
XP_024303298.1:p.Arg1820=
|
|
NM_002160.4:c.4911T>A
MANE Select
|
NP_002151.2:p.Arg1637=
|
|