ENST00000399820.8:c.813T>A
MANE Select
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ENSP00000382717.3:p.Ala271=
|
|
ENST00000399820.7:c.813T>A
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ENSP00000382717.3:p.Ala271=
|
|
ENST00000503697.5:c.*281T>A
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ENSP00000423706.1:n.*281T>A
|
|
ENST00000506503.1:c.813T>A
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ENSP00000423491.1:p.Ala271=
|
|
ENST00000506869.5:c.*394T>A
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ENSP00000424319.1:n.*394T>A
|
|
ENST00000511729.5:n.41-22899T>A
|
|
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ENST00000512448.1:n.407T>A
|
|
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NM_025132.3:c.813T>A
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NP_079408.3:p.Ala271=
|
|
XM_011513724.1:c.813T>A
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XP_011512026.1:p.Ala271=
|
|
XM_011513725.1:c.747T>A
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XP_011512027.1:p.Ala249=
|
|
XM_011513726.1:c.333T>A
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XP_011512028.1:p.Ala111=
|
|
XM_011513727.1:c.333T>A
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XP_011512029.1:p.Ala111=
|
|
XM_011513728.1:c.333T>A
|
XP_011512030.1:p.Ala111=
|
|
XM_011513729.1:c.813T>A
|
XP_011512031.1:p.Ala271=
|
|
XR_925155.1:n.877T>A
|
|
|
NM_001317924.1:c.333T>A
|
NP_001304853.1:p.Ala111=
|
|
XM_011513725.2:c.747T>A
|
XP_011512027.1:p.Ala249=
|
|
XM_011513726.3:c.333T>A
|
XP_011512028.1:p.Ala111=
|
|
XM_017008501.1:c.333T>A
|
XP_016863990.1:p.Ala111=
|
|
XR_001741306.1:n.877T>A
|
|
|
XR_001741307.1:n.877T>A
|
|
|
XR_001741308.1:n.877T>A
|
|
|
XR_001741309.1:n.877T>A
|
|
|
XR_001741310.1:n.877T>A
|
|
|
XR_001741311.2:n.726T>A
|
|
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XR_001741312.1:n.877T>A
|
|
|
NM_025132.4:c.813T>A
MANE Select
|
NP_079408.3:p.Ala271=
|
|
NM_001317924.2:c.333T>A
|
NP_001304853.1:p.Ala111=
|
|