ENST00000261693.11:c.*1711A>G
MANE Select
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ENSP00000261693.6:n.*1711A>G
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ENST00000339570.9:c.*1591A>G
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ENSP00000343795.4:n.*1591A>G
|
|
NM_005505.5:c.*1711A>G
MANE Select
|
NP_005496.4:n.*1711A>G
|
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NM_001082959.2:c.*1591A>G
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NP_001076428.1:n.*1591A>G
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|
NM_001367981.1:c.*1703A>G
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NP_001354910.1:n.*1703A>G
|
|
NM_001367983.1:c.*1711A>G
|
NP_001354912.1:n.*1711A>G
|
|
NM_001367984.1:c.*1711A>G
|
NP_001354913.1:n.*1711A>G
|
|
NM_001367985.1:c.*1711A>G
|
NP_001354914.1:n.*1711A>G
|
|
NM_001367986.1:c.*1711A>G
|
NP_001354915.1:n.*1711A>G
|
|
NM_001367987.1:c.*1591A>G
|
NP_001354916.1:n.*1591A>G
|
|
NM_001367988.1:c.*1711A>G
|
NP_001354917.1:n.*1711A>G
|
|
NM_001367989.1:c.*1722A>G
|
NP_001354918.1:n.*1722A>G
|
|
NR_160416.1:n.3386A>G
|
|
|
NR_160417.1:n.3488A>G
|
|
|
NR_160418.1:n.2947A>G
|
|
|
NR_160419.1:n.3311A>G
|
|
|
NR_160420.1:n.3140A>G
|
|
|
NR_160421.1:n.3063A>G
|
|
|
NR_160422.1:n.3269A>G
|
|
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NR_160423.1:n.3266A>G
|
|
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NR_160424.1:n.3251A>G
|
|
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