ENST00000255078.8:c.2391A>T
MANE Select
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ENSP00000255078.4:p.Ala797=
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ENST00000674675.1:c.587+48A>T
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ENST00000674878.1:c.548-52A>T
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ENST00000675118.1:c.1879A>T
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|
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ENST00000675389.1:n.666A>T
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ENST00000675615.1:c.2391A>T
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ENSP00000502413.1:p.Ala797=
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ENST00000675648.1:n.1766A>T
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ENST00000675916.1:c.635A>T
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ENST00000676173.1:n.3136A>T
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ENST00000676182.1:c.822A>T
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ENST00000676228.1:c.*1714A>T
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ENSP00000502375.1:n.*1714A>T
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ENST00000255078.7:c.2391A>T
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ENSP00000255078.3:p.Ala797=
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ENST00000539064.5:n.2150A>T
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ENST00000543739.5:n.1384A>T
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NM_002180.2:c.2391A>T , LRG_250t1:c.2391A>T
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NP_002171.2:p.Ala797=
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XM_005273974.2:c.1380A>T
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XP_005274031.1:p.Ala460=
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XM_005273975.2:c.1263A>T
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XP_005274032.1:p.Ala421=
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XM_011544994.1:c.1158A>T
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XP_011543296.1:p.Ala386=
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XR_949903.1:n.2493A>T
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|
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XM_005273975.3:c.1263A>T
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XP_005274032.1:p.Ala421=
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XM_017017669.2:c.1380A>T
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XP_016873158.1:p.Ala460=
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XM_017017670.2:c.1380A>T
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XP_016873159.1:p.Ala460=
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XR_949903.3:n.2489A>T
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|
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NM_002180.3:c.2391A>T
MANE Select
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NP_002171.2:p.Ala797=
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