ENST00000449606.7:c.787G>T
MANE Select
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ENSP00000395196.2:p.Ala263Ser
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ENST00000674054.1:c.787G>T
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ENSP00000501251.1:p.Ala263Ser
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ENST00000449606.5:c.787G>T
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ENSP00000395196.1:p.Ala263Ser
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ENST00000562402.1:n.391G>T
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ENST00000563232.1:c.787G>T
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ENSP00000456218.1:p.Ala263Ser
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ENST00000563459.5:c.787G>T
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ENSP00000456467.1:p.Ala263Ser
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ENST00000564501.5:c.787G>T
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ENSP00000457107.1:p.Ala263Ser
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ENST00000564987.1:n.411G>T
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ENST00000565344.1:n.160G>T
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NM_001083614.1:c.787G>T
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NP_001077083.1:p.Ala263Ser
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NM_001308211.1:c.787G>T
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NP_001295140.1:p.Ala263Ser
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NR_003501.1:n.819G>T
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|
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XM_011545738.1:c.715G>T
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XP_011544040.1:p.Ala239Ser
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XM_011545739.1:c.508G>T
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XP_011544041.1:p.Ala170Ser
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XR_001751841.1:n.1109G>T
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|
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NM_001083614.2:c.787G>T
MANE Select
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NP_001077083.1:p.Ala263Ser
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NR_003501.2:n.794G>T
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