ENST00000264595.7:c.406G>A
MANE Select
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ENSP00000264595.2:p.Ala136Thr
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ENST00000264595.6:c.406G>A
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ENSP00000264595.2:p.Ala136Thr
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ENST00000502310.5:c.61G>A
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ENSP00000423798.1:p.Ala21Thr
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ENST00000506853.5:n.440G>A
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ENST00000510635.1:c.102G>A
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ENST00000510955.5:n.327G>A
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NM_000027.3:c.406G>A
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NP_000018.2:p.Ala136Thr
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NM_001171988.1:c.406G>A
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NP_001165459.1:p.Ala136Thr
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NR_033655.1:n.534G>A
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XM_006714123.2:c.406G>A
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XP_006714186.1:p.Ala136Thr
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XR_001741155.2:n.500G>A
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NM_000027.4:c.406G>A
MANE Select
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NP_000018.2:p.Ala136Thr
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NM_001171988.2:c.406G>A
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NP_001165459.1:p.Ala136Thr
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NR_033655.2:n.468G>A
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