ENST00000350721.9:c.7787A>T
MANE Select
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ENSP00000343741.4:p.Glu2596Val
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ENST00000513291.2:n.6496A>T
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ENST00000653893.1:n.2645A>T
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ENST00000654170.1:n.2630A>T
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ENST00000656114.1:n.2873A>T
|
|
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ENST00000656590.1:c.6714A>T
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ENST00000658083.1:n.2967A>T
|
|
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ENST00000661310.1:c.7595A>T
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ENSP00000499589.1:p.Glu2532Val
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ENST00000665483.1:n.5327A>T
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ENST00000666447.1:n.4290A>T
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ENST00000666943.1:n.4519A>T
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ENST00000350721.8:c.7787A>T
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ENSP00000343741.4:p.Glu2596Val
|
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ENST00000504521.5:c.376A>T
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ENSP00000422553.1:n.376A>T
|
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ENST00000513291.1:c.4851A>T
|
|
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ENST00000515810.1:c.213A>T
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ENSP00000421870.1:n.213A>T
|
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NM_001184.3:c.7787A>T
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NP_001175.2:p.Glu2596Val
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XM_011512924.1:c.7793A>T
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XP_011511226.1:p.Glu2598Val
|
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XM_011512925.1:c.7601A>T
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XP_011511227.1:p.Glu2534Val
|
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XR_924147.1:n.10544A>T
|
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XR_924148.1:n.8019A>T
|
|
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NM_001354579.1:c.7595A>T
|
NP_001341508.1:p.Glu2532Val
|
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XR_001740179.2:n.8013A>T
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XR_924148.2:n.8019A>T
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|
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NM_001184.4:c.7787A>T
MANE Select
|
NP_001175.2:p.Glu2596Val
|
|
NM_001354579.2:c.7595A>T
|
NP_001341508.1:p.Glu2532Val
|
|