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ENST00000476680.2:c.318-4152G=
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ENST00000537320.6:c.3215-4152G=
|
ENSP00000443478.1:n.3215-4152G=
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ENST00000542877.6:c.3953G=
|
ENSP00000442242.1:p.Arg1318=
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ENST00000705190.1:c.1985G=
|
ENSP00000516083.1:p.Arg662=
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ENST00000705191.1:c.641G=
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ENSP00000516084.1:p.Arg214=
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ENST00000705192.1:c.4000G=
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ENST00000350763.9:c.5042G=
MANE Select
|
ENSP00000265131.4:p.Arg1681=
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ENST00000341037.8:c.4496G=
|
ENSP00000339553.4:p.Arg1499=
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ENST00000350763.8:c.5042G=
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ENSP00000265131.4:p.Arg1681=
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ENST00000423613.6:c.4307-4152G=
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ENSP00000411406.2:n.4307-4152G=
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ENST00000473855.1:n.360G=
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ENST00000476680.1:n.253-4152G=
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ENST00000498724.5:n.40-4152G=
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ENST00000535648.5:c.3953G=
|
ENSP00000438152.2:p.Arg1318=
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ENST00000537320.5:c.3215-4152G=
|
ENSP00000443478.1:n.3215-4152G=
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ENST00000542877.5:c.3953G=
|
ENSP00000442242.1:p.Arg1318=
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ENST00000544972.1:c.729G=
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NM_002160.3:c.5042G=
|
NP_002151.2:p.Arg1681=
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XM_005251972.2:c.4769G=
|
XP_005252029.1:p.Arg1590=
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XM_005251973.2:c.4034-4152G=
|
XP_005252030.1:n.4034-4152G=
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XM_005251974.2:c.3404G=
|
XP_005252031.1:p.Arg1135=
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XM_005251975.2:c.3215-4152G=
|
XP_005252032.1:n.3215-4152G=
|
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XM_006717096.2:c.5318G=
|
XP_006717159.1:p.Arg1773=
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XM_006717097.2:c.4769G=
|
XP_006717160.1:p.Arg1590=
|
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XM_006717098.2:c.4496G=
|
XP_006717161.1:p.Arg1499=
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XM_006717100.2:c.4307-4152G=
|
XP_006717163.1:n.4307-4152G=
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XM_006717101.2:c.3488-4152G=
|
XP_006717164.1:n.3488-4152G=
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XM_011518622.1:c.5045G=
|
XP_011516924.1:p.Arg1682=
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XM_011518623.1:c.5045G=
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XP_011516925.1:p.Arg1682=
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XM_011518624.1:c.4499G=
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XP_011516926.1:p.Arg1500=
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XM_011518625.1:c.4580-4152G=
|
XP_011516927.1:n.4580-4152G=
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XM_011518626.1:c.4226G=
|
XP_011516928.1:p.Arg1409=
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XM_011518627.1:c.3953G=
|
XP_011516929.1:p.Arg1318=
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XM_011518628.1:c.3761-4152G=
|
XP_011516930.1:n.3761-4152G=
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XM_011518629.1:c.3677G=
|
XP_011516931.1:p.Arg1226=
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XM_005251972.4:c.4769G=
|
XP_005252029.1:p.Arg1590=
|
|
|
XM_005251973.4:c.4034-4152G=
|
XP_005252030.1:n.4034-4152G=
|
|
|
XM_005251974.4:c.3404G=
|
XP_005252031.1:p.Arg1135=
|
|
|
XM_005251975.4:c.3215-4152G=
|
XP_005252032.1:n.3215-4152G=
|
|
|
XM_006717096.4:c.5318G=
|
XP_006717159.1:p.Arg1773=
|
|
|
XM_006717097.4:c.4769G=
|
XP_006717160.1:p.Arg1590=
|
|
|
XM_006717098.4:c.4496G=
|
XP_006717161.1:p.Arg1499=
|
|
|
XM_006717101.4:c.3488-4152G=
|
XP_006717164.1:n.3488-4152G=
|
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|
XM_011518625.3:c.4580-4152G=
|
XP_011516927.1:n.4580-4152G=
|
|
|
XM_011518626.3:c.4226G=
|
XP_011516928.1:p.Arg1409=
|
|
|
XM_011518628.3:c.3761-4152G=
|
XP_011516930.1:n.3761-4152G=
|
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|
XM_011518629.3:c.3677G=
|
XP_011516931.1:p.Arg1226=
|
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|
XM_017014678.2:c.5591G=
|
XP_016870167.1:p.Arg1864=
|
|
|
XM_017014679.2:c.5318G=
|
XP_016870168.1:p.Arg1773=
|
|
|
XM_017014680.2:c.5315G=
|
XP_016870169.1:p.Arg1772=
|
|
|
XM_017014681.2:c.4499G=
|
XP_016870170.1:p.Arg1500=
|
|
|
XM_024447530.1:c.5591G=
|
XP_024303298.1:p.Arg1864=
|
|
|
NM_002160.4:c.5042G=
MANE Select
|
NP_002151.2:p.Arg1681=
|
|
