ENST00000265631.10:c.1393G>T
MANE Select
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ENSP00000265631.6:p.Gly465Cys
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ENST00000265631.9:c.1393G>T
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ENSP00000265631.5:p.Gly465Cys
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ENST00000416240.6:c.1396G>T
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ENSP00000400101.2:p.Gly466Cys
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ENST00000490072.5:n.517G>T
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NM_001160210.1:c.1396G>T
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NP_001153682.1:p.Gly466Cys
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NM_014251.2:c.1393G>T
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NP_055066.1:p.Gly465Cys
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NR_027662.1:n.1468G>T
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XM_006715831.2:c.1426G>T
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XP_006715894.1:p.Gly476Cys
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XM_011515728.1:c.541G>T
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XP_011514030.1:p.Gly181Cys
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XM_006715831.4:c.1426G>T
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XP_006715894.1:p.Gly476Cys
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XM_011515727.3:c.*130G>T
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XP_011514029.1:n.*130G>T
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XM_017011663.1:c.1384G>T
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XP_016867152.1:p.Gly462Cys
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XM_017011664.2:c.541G>T
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XP_016867153.1:p.Gly181Cys
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XM_017011665.1:c.541G>T
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XP_016867154.1:p.Gly181Cys
|
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XR_001744525.2:n.1639G>T
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XR_002956405.1:n.2197G>T
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|
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NM_014251.3:c.1393G>T
MANE Select
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NP_055066.1:p.Gly465Cys
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NR_027662.2:n.1419G>T
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NM_001160210.2:c.1396G>T
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NP_001153682.1:p.Gly466Cys
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