ENST00000476680.2:c.318-4145T>C
|
|
|
ENST00000537320.6:c.3215-4145T>C
|
ENSP00000443478.1:n.3215-4145T>C
|
|
ENST00000542877.6:c.3960T>C
|
ENSP00000442242.1:p.Ala1320=
|
|
ENST00000705190.1:c.1992T>C
|
ENSP00000516083.1:p.Ala664=
|
|
ENST00000705191.1:c.648T>C
|
ENSP00000516084.1:p.Ala216=
|
|
ENST00000705192.1:c.4007T>C
|
|
|
ENST00000350763.9:c.5049T>C
MANE Select
|
ENSP00000265131.4:p.Ala1683=
|
|
ENST00000341037.8:c.4503T>C
|
ENSP00000339553.4:p.Ala1501=
|
|
ENST00000350763.8:c.5049T>C
|
ENSP00000265131.4:p.Ala1683=
|
|
ENST00000423613.6:c.4307-4145T>C
|
ENSP00000411406.2:n.4307-4145T>C
|
|
ENST00000473855.1:n.367T>C
|
|
|
ENST00000476680.1:n.253-4145T>C
|
|
|
ENST00000498724.5:n.40-4145T>C
|
|
|
ENST00000535648.5:c.3960T>C
|
ENSP00000438152.2:p.Ala1320=
|
|
ENST00000537320.5:c.3215-4145T>C
|
ENSP00000443478.1:n.3215-4145T>C
|
|
ENST00000542877.5:c.3960T>C
|
ENSP00000442242.1:p.Ala1320=
|
|
ENST00000544972.1:c.736T>C
|
|
|
NM_002160.3:c.5049T>C
|
NP_002151.2:p.Ala1683=
|
|
XM_005251972.2:c.4776T>C
|
XP_005252029.1:p.Ala1592=
|
|
XM_005251973.2:c.4034-4145T>C
|
XP_005252030.1:n.4034-4145T>C
|
|
XM_005251974.2:c.3411T>C
|
XP_005252031.1:p.Ala1137=
|
|
XM_005251975.2:c.3215-4145T>C
|
XP_005252032.1:n.3215-4145T>C
|
|
XM_006717096.2:c.5325T>C
|
XP_006717159.1:p.Ala1775=
|
|
XM_006717097.2:c.4776T>C
|
XP_006717160.1:p.Ala1592=
|
|
XM_006717098.2:c.4503T>C
|
XP_006717161.1:p.Ala1501=
|
|
XM_006717100.2:c.4307-4145T>C
|
XP_006717163.1:n.4307-4145T>C
|
|
XM_006717101.2:c.3488-4145T>C
|
XP_006717164.1:n.3488-4145T>C
|
|
XM_011518622.1:c.5052T>C
|
XP_011516924.1:p.Ala1684=
|
|
XM_011518623.1:c.5052T>C
|
XP_011516925.1:p.Ala1684=
|
|
XM_011518624.1:c.4506T>C
|
XP_011516926.1:p.Ala1502=
|
|
XM_011518625.1:c.4580-4145T>C
|
XP_011516927.1:n.4580-4145T>C
|
|
XM_011518626.1:c.4233T>C
|
XP_011516928.1:p.Ala1411=
|
|
XM_011518627.1:c.3960T>C
|
XP_011516929.1:p.Ala1320=
|
|
XM_011518628.1:c.3761-4145T>C
|
XP_011516930.1:n.3761-4145T>C
|
|
XM_011518629.1:c.3684T>C
|
XP_011516931.1:p.Ala1228=
|
|
XM_005251972.4:c.4776T>C
|
XP_005252029.1:p.Ala1592=
|
|
XM_005251973.4:c.4034-4145T>C
|
XP_005252030.1:n.4034-4145T>C
|
|
XM_005251974.4:c.3411T>C
|
XP_005252031.1:p.Ala1137=
|
|
XM_005251975.4:c.3215-4145T>C
|
XP_005252032.1:n.3215-4145T>C
|
|
XM_006717096.4:c.5325T>C
|
XP_006717159.1:p.Ala1775=
|
|
XM_006717097.4:c.4776T>C
|
XP_006717160.1:p.Ala1592=
|
|
XM_006717098.4:c.4503T>C
|
XP_006717161.1:p.Ala1501=
|
|
XM_006717101.4:c.3488-4145T>C
|
XP_006717164.1:n.3488-4145T>C
|
|
XM_011518625.3:c.4580-4145T>C
|
XP_011516927.1:n.4580-4145T>C
|
|
XM_011518626.3:c.4233T>C
|
XP_011516928.1:p.Ala1411=
|
|
XM_011518628.3:c.3761-4145T>C
|
XP_011516930.1:n.3761-4145T>C
|
|
XM_011518629.3:c.3684T>C
|
XP_011516931.1:p.Ala1228=
|
|
XM_017014678.2:c.5598T>C
|
XP_016870167.1:p.Ala1866=
|
|
XM_017014679.2:c.5325T>C
|
XP_016870168.1:p.Ala1775=
|
|
XM_017014680.2:c.5322T>C
|
XP_016870169.1:p.Ala1774=
|
|
XM_017014681.2:c.4506T>C
|
XP_016870170.1:p.Ala1502=
|
|
XM_024447530.1:c.5598T>C
|
XP_024303298.1:p.Ala1866=
|
|
NM_002160.4:c.5049T>C
MANE Select
|
NP_002151.2:p.Ala1683=
|
|