ENST00000350721.9:c.4636C>G
MANE Select
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ENSP00000343741.4:p.Gln1546Glu
|
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ENST00000653868.1:n.4665C>G
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|
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ENST00000656590.1:c.3426C>G
|
|
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ENST00000661310.1:c.4444C>G
|
ENSP00000499589.1:p.Gln1482Glu
|
|
ENST00000666943.1:n.100C>G
|
|
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ENST00000350721.8:c.4636C>G
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ENSP00000343741.4:p.Gln1546Glu
|
|
NM_001184.3:c.4636C>G
|
NP_001175.2:p.Gln1546Glu
|
|
XM_011512924.1:c.4642C>G
|
XP_011511226.1:p.Gln1548Glu
|
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XM_011512925.1:c.4450C>G
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XP_011511227.1:p.Gln1484Glu
|
|
XM_011512926.1:c.4642C>G
|
XP_011511228.1:p.Gln1548Glu
|
|
XM_011512927.1:c.4642C>G
|
XP_011511229.1:p.Gln1548Glu
|
|
XR_924147.1:n.4731C>G
|
|
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XR_924148.1:n.4731C>G
|
|
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XR_924149.1:n.4731C>G
|
|
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NM_001354579.1:c.4444C>G
|
NP_001341508.1:p.Gln1482Glu
|
|
XR_001740179.2:n.4725C>G
|
|
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XR_001740180.2:n.4731C>G
|
|
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XR_001740181.2:n.4731C>G
|
|
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XR_001740182.1:n.4731C>G
|
|
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XR_002959543.1:n.4731C>G
|
|
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XR_924148.2:n.4731C>G
|
|
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NM_001184.4:c.4636C>G
MANE Select
|
NP_001175.2:p.Gln1546Glu
|
|
NM_001354579.2:c.4444C>G
|
NP_001341508.1:p.Gln1482Glu
|
|