ENST00000378106.10:c.613G>C
MANE Select
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ENSP00000367346.5:p.Glu205Gln
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ENST00000378081.9:c.613G>C
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ENSP00000437325.1:p.Glu205Gln
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ENST00000378106.9:c.613G>C
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ENSP00000367346.5:p.Glu205Gln
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ENST00000463598.1:c.529G>C
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ENSP00000420497.1:p.Glu177Gln
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ENST00000464269.5:n.286G>C
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ENST00000475968.5:n.490G>C
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ENST00000476124.1:n.12G>C
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ENST00000476536.5:n.573G>C
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|
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ENST00000477732.5:n.502+3079G>C
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ENST00000479716.5:n.134G>C
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ENST00000481249.5:n.490G>C
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ENST00000485738.5:n.590G>C
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|
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ENST00000487478.5:n.37G>C
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NM_001039375.2:c.529G>C
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NP_001034464.1:p.Glu177Gln
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NM_024120.4:c.613G>C
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NP_077025.2:p.Glu205Gln
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NR_029377.1:n.656G>C
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|
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XM_006723620.2:c.613G>C
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XP_006723683.1:p.Glu205Gln
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XM_006723622.2:c.142G>C
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XP_006723685.1:p.Glu48Gln
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XM_006723623.1:c.142G>C
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XP_006723686.1:p.Glu48Gln
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XM_006723624.1:c.142G>C
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XP_006723687.1:p.Glu48Gln
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XM_011529341.1:c.613G>C
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XP_011527643.1:p.Glu205Gln
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XM_011529342.1:c.613G>C
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XP_011527644.1:p.Glu205Gln
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XM_011529343.1:c.613G>C
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XP_011527645.1:p.Glu205Gln
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|
XM_011529344.1:c.244G>C
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XP_011527646.1:p.Glu82Gln
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XR_430269.2:n.633G>C
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|
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XR_937140.1:n.633G>C
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NM_001352403.1:c.142G>C
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NP_001339332.1:p.Glu48Gln
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|
NM_001352406.1:c.52G>C
|
NP_001339335.1:p.Glu18Gln
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|
NM_001352407.1:c.52G>C
|
NP_001339336.1:p.Glu18Gln
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NM_001352408.1:c.613G>C
|
NP_001339337.1:p.Glu205Gln
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NR_147978.1:n.656G>C
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|
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NR_147979.1:n.676G>C
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NR_147980.1:n.552G>C
|
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NR_147981.1:n.790G>C
|
|
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NR_147982.1:n.790G>C
|
|
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NR_147983.1:n.706G>C
|
|
|
XM_006723624.2:c.142G>C
|
XP_006723687.1:p.Glu48Gln
|
|
XM_011529342.2:c.613G>C
|
XP_011527644.1:p.Glu205Gln
|
|
XM_024451999.1:c.142G>C
|
XP_024307767.1:p.Glu48Gln
|
|
XR_001754396.1:n.572G>C
|
|
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XR_430269.3:n.633G>C
|
|
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XR_937140.2:n.633G>C
|
|
|
NM_024120.5:c.613G>C
MANE Select
|
NP_077025.2:p.Glu205Gln
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|
NM_001039375.3:c.529G>C
|
NP_001034464.1:p.Glu177Gln
|
|
NM_001352403.2:c.142G>C
|
NP_001339332.1:p.Glu48Gln
|
|
NM_001352406.2:c.52G>C
|
NP_001339335.1:p.Glu18Gln
|
|
NM_001352407.2:c.52G>C
|
NP_001339336.1:p.Glu18Gln
|
|
NR_029377.2:n.654G>C
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|
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NR_147978.2:n.654G>C
|
|
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NR_147979.2:n.674G>C
|
|
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NR_147980.2:n.550G>C
|
|
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NR_147981.2:n.788G>C
|
|
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NR_147982.2:n.788G>C
|
|
|
NR_147983.2:n.704G>C
|
|
|
NM_001352408.2:c.613G>C
|
NP_001339337.1:p.Glu205Gln
|
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