ENST00000220616.9:c.8075C>T
MANE Select
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ENSP00000220616.4:p.Ala2692Val
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ENST00000220616.8:c.8075C>T
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ENSP00000220616.4:p.Ala2692Val
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ENST00000519178.5:c.3441C>T
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ENST00000519543.5:c.2474C>T
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ENSP00000430430.1:p.Ala825Val
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ENST00000521107.1:c.287C>T
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ENSP00000430161.1:p.Ala96Val
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ENST00000522691.1:n.161C>T
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|
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ENST00000523756.5:c.4730C>T
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NM_003235.4:c.8075C>T
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NP_003226.4:p.Ala2692Val
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XM_005251038.3:c.7883C>T
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XP_005251095.1:p.Ala2628Val
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XM_006716622.2:c.8012C>T
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XP_006716685.1:p.Ala2671Val
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XM_005251038.4:c.7883C>T
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XP_005251095.1:p.Ala2628Val
|
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XM_006716622.3:c.8012C>T
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XP_006716685.1:p.Ala2671Val
|
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XM_017013793.1:c.8009C>T
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XP_016869282.1:p.Ala2670Val
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XM_017013794.1:c.7940C>T
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XP_016869283.1:p.Ala2647Val
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XM_017013795.1:c.7904C>T
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XP_016869284.1:p.Ala2635Val
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XM_017013796.1:c.7856C>T
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XP_016869285.1:p.Ala2619Val
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XM_017013797.1:c.7814C>T
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XP_016869286.1:p.Ala2605Val
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NM_003235.5:c.8075C>T
MANE Select
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NP_003226.4:p.Ala2692Val
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