ENST00000255078.8:c.2392G>A
MANE Select
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ENSP00000255078.4:p.Gly798Arg
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ENST00000674675.1:c.587+49G>A
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ENST00000674878.1:c.548-51G>A
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ENST00000675118.1:c.1880G>A
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ENST00000675389.1:n.667G>A
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ENST00000675615.1:c.2392G>A
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ENSP00000502413.1:p.Gly798Arg
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ENST00000675648.1:n.1767G>A
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ENST00000675916.1:c.636G>A
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ENST00000676173.1:n.3137G>A
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ENST00000676182.1:c.823G>A
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ENST00000676228.1:c.*1715G>A
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ENSP00000502375.1:n.*1715G>A
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ENST00000255078.7:c.2392G>A
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ENSP00000255078.3:p.Gly798Arg
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ENST00000539064.5:n.2151G>A
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ENST00000543739.5:n.1385G>A
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NM_002180.2:c.2392G>A , LRG_250t1:c.2392G>A
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NP_002171.2:p.Gly798Arg
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XM_005273974.2:c.1381G>A
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XP_005274031.1:p.Gly461Arg
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XM_005273975.2:c.1264G>A
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XP_005274032.1:p.Gly422Arg
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XM_011544994.1:c.1159G>A
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XP_011543296.1:p.Gly387Arg
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XR_949903.1:n.2494G>A
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XM_005273975.3:c.1264G>A
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XP_005274032.1:p.Gly422Arg
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XM_017017669.2:c.1381G>A
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XP_016873158.1:p.Gly461Arg
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XM_017017670.2:c.1381G>A
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XP_016873159.1:p.Gly461Arg
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XR_949903.3:n.2490G>A
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NM_002180.3:c.2392G>A
MANE Select
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NP_002171.2:p.Gly798Arg
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