ENST00000348332.8:c.*249T>C
MANE Select
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ENSP00000320940.5:n.*249T>C
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ENST00000288599.9:c.*432T>C
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ENSP00000288599.5:n.*432T>C
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ENST00000348332.7:c.*249T>C
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ENSP00000320940.5:n.*249T>C
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ENST00000395856.3:c.*249T>C
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ENSP00000379197.3:n.*249T>C
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ENST00000405141.5:c.*432T>C
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ENSP00000385097.1:n.*432T>C
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ENST00000406961.5:c.*249T>C
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ENSP00000385216.1:n.*249T>C
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NM_003743.4:c.*249T>C
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NP_003734.3:n.*249T>C
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NM_147223.2:c.*432T>C
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NP_671756.1:n.*432T>C
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NM_147233.2:c.*249T>C
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NP_671766.1:n.*249T>C
|
|
XM_005264625.1:c.*249T>C
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XP_005264682.1:n.*249T>C
|
|
XM_005264626.1:c.*249T>C
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XP_005264683.1:n.*249T>C
|
|
XM_005264627.1:c.*432T>C
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XP_005264684.1:n.*432T>C
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XM_005264628.1:c.*429T>C
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XP_005264685.1:n.*429T>C
|
|
XM_011533141.1:c.*249T>C
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XP_011531443.1:n.*249T>C
|
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NM_001362950.1:c.*432T>C
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NP_001349879.1:n.*432T>C
|
|
NM_001362952.1:c.*432T>C
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NP_001349881.1:n.*432T>C
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NM_001362954.1:c.*429T>C
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NP_001349883.1:n.*429T>C
|
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NM_001362955.1:c.*432T>C
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NP_001349884.1:n.*432T>C
|
|
NM_003743.5:c.*249T>C
MANE Select
|
NP_003734.3:n.*249T>C
|
|
NM_147223.3:c.*432T>C
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NP_671756.1:n.*432T>C
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