ENST00000378106.10:c.701T>G
MANE Select
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ENSP00000367346.5:p.Phe234Cys
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ENST00000378081.9:c.701T>G
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ENSP00000437325.1:p.Phe234Cys
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ENST00000378106.9:c.701T>G
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ENSP00000367346.5:p.Phe234Cys
|
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ENST00000463598.1:c.617T>G
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ENSP00000420497.1:p.Phe206Cys
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ENST00000464269.5:n.374T>G
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ENST00000475968.5:n.578T>G
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|
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ENST00000476124.1:n.100T>G
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ENST00000476536.5:n.661T>G
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|
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ENST00000477732.5:n.502+3167T>G
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|
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ENST00000479716.5:n.222T>G
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|
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ENST00000481249.5:n.578T>G
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|
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ENST00000485738.5:n.678T>G
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|
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ENST00000487478.5:n.125T>G
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NM_001039375.2:c.617T>G
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NP_001034464.1:p.Phe206Cys
|
|
NM_024120.4:c.701T>G
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NP_077025.2:p.Phe234Cys
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NR_029377.1:n.744T>G
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|
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XM_006723620.2:c.701T>G
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XP_006723683.1:p.Phe234Cys
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XM_006723622.2:c.230T>G
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XP_006723685.1:p.Phe77Cys
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XM_006723623.1:c.230T>G
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XP_006723686.1:p.Phe77Cys
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XM_006723624.1:c.230T>G
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XP_006723687.1:p.Phe77Cys
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XM_011529341.1:c.701T>G
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XP_011527643.1:p.Phe234Cys
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|
XM_011529342.1:c.701T>G
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XP_011527644.1:p.Phe234Cys
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|
XM_011529343.1:c.701T>G
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XP_011527645.1:p.Phe234Cys
|
|
XM_011529344.1:c.332T>G
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XP_011527646.1:p.Phe111Cys
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XR_430269.2:n.721T>G
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XR_937140.1:n.721T>G
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NM_001352403.1:c.230T>G
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NP_001339332.1:p.Phe77Cys
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|
NM_001352406.1:c.140T>G
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NP_001339335.1:p.Phe47Cys
|
|
NM_001352407.1:c.140T>G
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NP_001339336.1:p.Phe47Cys
|
|
NM_001352408.1:c.701T>G
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NP_001339337.1:p.Phe234Cys
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NR_147978.1:n.744T>G
|
|
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NR_147979.1:n.764T>G
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NR_147980.1:n.640T>G
|
|
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NR_147981.1:n.878T>G
|
|
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NR_147982.1:n.878T>G
|
|
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NR_147983.1:n.794T>G
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XM_006723624.2:c.230T>G
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XP_006723687.1:p.Phe77Cys
|
|
XM_011529342.2:c.701T>G
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XP_011527644.1:p.Phe234Cys
|
|
XM_024451999.1:c.230T>G
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XP_024307767.1:p.Phe77Cys
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|
XR_001754396.1:n.660T>G
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|
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XR_430269.3:n.721T>G
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|
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XR_937140.2:n.721T>G
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|
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NM_024120.5:c.701T>G
MANE Select
|
NP_077025.2:p.Phe234Cys
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|
NM_001039375.3:c.617T>G
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NP_001034464.1:p.Phe206Cys
|
|
NM_001352403.2:c.230T>G
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NP_001339332.1:p.Phe77Cys
|
|
NM_001352406.2:c.140T>G
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NP_001339335.1:p.Phe47Cys
|
|
NM_001352407.2:c.140T>G
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NP_001339336.1:p.Phe47Cys
|
|
NR_029377.2:n.742T>G
|
|
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NR_147978.2:n.742T>G
|
|
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NR_147979.2:n.762T>G
|
|
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NR_147980.2:n.638T>G
|
|
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NR_147981.2:n.876T>G
|
|
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NR_147982.2:n.876T>G
|
|
|
NR_147983.2:n.792T>G
|
|
|
NM_001352408.2:c.701T>G
|
NP_001339337.1:p.Phe234Cys
|
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