ENST00000220616.9:c.8186C>T
MANE Select
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ENSP00000220616.4:p.Ala2729Val
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ENST00000220616.8:c.8186C>T
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ENSP00000220616.4:p.Ala2729Val
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ENST00000519178.5:c.3552C>T
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|
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ENST00000519543.5:c.2585C>T
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ENSP00000430430.1:p.Ala862Val
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ENST00000521107.1:c.398C>T
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ENSP00000430161.1:p.Ala133Val
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ENST00000522691.1:n.272C>T
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|
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ENST00000523756.5:c.4841C>T
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|
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NM_003235.4:c.8186C>T
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NP_003226.4:p.Ala2729Val
|
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XM_005251038.3:c.7994C>T
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XP_005251095.1:p.Ala2665Val
|
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XM_006716622.2:c.8123C>T
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XP_006716685.1:p.Ala2708Val
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XM_005251038.4:c.7994C>T
|
XP_005251095.1:p.Ala2665Val
|
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XM_006716622.3:c.8123C>T
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XP_006716685.1:p.Ala2708Val
|
|
XM_017013793.1:c.8120C>T
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XP_016869282.1:p.Ala2707Val
|
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XM_017013794.1:c.8051C>T
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XP_016869283.1:p.Ala2684Val
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XM_017013795.1:c.8015C>T
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XP_016869284.1:p.Ala2672Val
|
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XM_017013796.1:c.7967C>T
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XP_016869285.1:p.Ala2656Val
|
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XM_017013797.1:c.7925C>T
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XP_016869286.1:p.Ala2642Val
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NM_003235.5:c.8186C>T
MANE Select
|
NP_003226.4:p.Ala2729Val
|
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