ENST00000350721.9:c.7764C>G
MANE Select
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ENSP00000343741.4:p.Ala2588=
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ENST00000513291.2:n.6473C>G
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|
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ENST00000653893.1:n.2622C>G
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ENST00000654170.1:n.2607C>G
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ENST00000656114.1:n.2850C>G
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ENST00000656590.1:c.6691C>G
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ENST00000658083.1:n.2944C>G
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|
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ENST00000661310.1:c.7572C>G
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ENSP00000499589.1:p.Ala2524=
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ENST00000665483.1:n.5304C>G
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ENST00000666447.1:n.4267C>G
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ENST00000666943.1:n.4496C>G
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ENST00000350721.8:c.7764C>G
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ENSP00000343741.4:p.Ala2588=
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ENST00000504521.5:c.353C>G
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ENSP00000422553.1:n.353C>G
|
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ENST00000513291.1:c.4828C>G
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|
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ENST00000515810.1:c.190C>G
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ENSP00000421870.1:n.190C>G
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NM_001184.3:c.7764C>G
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NP_001175.2:p.Ala2588=
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XM_011512924.1:c.7770C>G
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XP_011511226.1:p.Ala2590=
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XM_011512925.1:c.7578C>G
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XP_011511227.1:p.Ala2526=
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XR_924147.1:n.10521C>G
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XR_924148.1:n.7996C>G
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NM_001354579.1:c.7572C>G
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NP_001341508.1:p.Ala2524=
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XR_001740179.2:n.7990C>G
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XR_924148.2:n.7996C>G
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NM_001184.4:c.7764C>G
MANE Select
|
NP_001175.2:p.Ala2588=
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NM_001354579.2:c.7572C>G
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NP_001341508.1:p.Ala2524=
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