ENST00000449606.7:c.796T>A
MANE Select
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ENSP00000395196.2:p.Trp266Arg
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ENST00000674054.1:c.796T>A
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ENSP00000501251.1:p.Trp266Arg
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ENST00000449606.5:c.796T>A
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ENSP00000395196.1:p.Trp266Arg
|
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ENST00000562402.1:n.400T>A
|
|
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ENST00000563232.1:c.796T>A
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ENSP00000456218.1:p.Trp266Arg
|
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ENST00000563459.5:c.796T>A
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ENSP00000456467.1:p.Trp266Arg
|
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ENST00000564501.5:c.796T>A
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ENSP00000457107.1:p.Trp266Arg
|
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ENST00000564987.1:n.420T>A
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|
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ENST00000565344.1:n.169T>A
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|
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NM_001083614.1:c.796T>A
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NP_001077083.1:p.Trp266Arg
|
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NM_001308211.1:c.796T>A
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NP_001295140.1:p.Trp266Arg
|
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NR_003501.1:n.828T>A
|
|
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XM_011545738.1:c.724T>A
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XP_011544040.1:p.Trp242Arg
|
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XM_011545739.1:c.517T>A
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XP_011544041.1:p.Trp173Arg
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XR_001751841.1:n.1118T>A
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|
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NM_001083614.2:c.796T>A
MANE Select
|
NP_001077083.1:p.Trp266Arg
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NR_003501.2:n.803T>A
|
|
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