ENST00000325366.14:c.74A>G
MANE Select
|
ENSP00000326879.9:p.His25Arg
|
|
ENST00000325366.13:c.74A>G
|
ENSP00000326879.9:p.His25Arg
|
|
ENST00000504464.5:c.74A>G
|
ENSP00000430261.1:p.His25Arg
|
|
ENST00000507818.6:c.74A>G
|
ENSP00000430860.1:p.His25Arg
|
|
ENST00000510659.5:c.74A>G
|
ENSP00000423039.1:p.His25Arg
|
|
ENST00000511208.2:c.74A>G
|
ENSP00000428898.1:p.His25Arg
|
|
ENST00000513967.5:c.74A>G
|
ENSP00000421667.1:p.His25Arg
|
|
ENST00000515409.5:n.172A>G
|
|
|
ENST00000517780.1:n.172A>G
|
|
|
NM_018356.2:c.74A>G
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NP_060826.2:p.His25Arg
|
|
XM_005248319.2:c.-498A>G
|
XP_005248376.1:n.-498A>G
|
|
XM_006714479.1:c.-87A>G
|
XP_006714542.1:n.-87A>G
|
|
XM_006714480.2:c.-409A>G
|
XP_006714543.1:n.-409A>G
|
|
XM_011514062.1:c.74A>G
|
XP_011512364.1:p.His25Arg
|
|
NR_134298.1:n.201A>G
|
|
|
XM_006714479.2:c.-87A>G
|
XP_006714542.1:n.-87A>G
|
|
XM_006714480.3:c.-409A>G
|
XP_006714543.1:n.-409A>G
|
|
XM_011514062.3:c.74A>G
|
XP_011512364.1:p.His25Arg
|
|
XM_017009607.1:c.74A>G
|
XP_016865096.1:p.His25Arg
|
|
XM_017009608.2:c.74A>G
|
XP_016865097.1:p.His25Arg
|
|
XM_017009609.1:c.-87A>G
|
XP_016865098.1:n.-87A>G
|
|
XM_017009610.1:c.-501A>G
|
XP_016865099.1:n.-501A>G
|
|
XM_017009611.2:c.-498A>G
|
XP_016865100.1:n.-498A>G
|
|
XM_017009612.2:c.-409A>G
|
XP_016865101.1:n.-409A>G
|
|
XM_017009613.2:c.-501A>G
|
XP_016865102.1:n.-501A>G
|
|
XM_017009614.1:c.-594A>G
|
XP_016865103.1:n.-594A>G
|
|
XM_017009615.1:c.-502A>G
|
XP_016865104.1:n.-502A>G
|
|
XM_017009616.1:c.-406A>G
|
XP_016865105.1:n.-406A>G
|
|
NM_018356.3:c.74A>G
MANE Select
|
NP_060826.2:p.His25Arg
|
|
NR_134298.2:n.166A>G
|
|
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