ENST00000209873.9:c.1501G>T
MANE Select
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ENSP00000209873.4:p.Ala501Ser
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ENST00000546562.6:n.2565G>T
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ENST00000547238.6:n.2137G>T
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ENST00000547520.6:n.1617G>T
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ENST00000547757.2:c.*419G>T
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ENSP00000448020.2:n.*419G>T
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ENST00000548931.6:c.936G>T
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ENSP00000457518.1:p.Gly312=
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ENST00000549450.6:n.1435G>T
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ENST00000672797.1:n.1990G>T
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ENST00000209873.8:c.1501G>T
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ENSP00000209873.4:p.Ala501Ser
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ENST00000394384.7:c.1402G>T
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ENSP00000377908.3:p.Ala468Ser
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ENST00000548931.5:c.936G>T
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ENSP00000457518.1:p.Gly312=
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ENST00000550286.5:c.1129G>T
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ENSP00000446885.1:p.Ala377Ser
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ENST00000552876.5:n.1844G>T
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|
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NM_001173466.1:c.1402G>T
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NP_001166937.1:p.Ala468Ser
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NM_015665.5:c.1501G>T
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NP_056480.1:p.Ala501Ser
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XM_006719617.2:c.1516G>T
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XP_006719680.1:p.Ala506Ser
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XM_011538777.1:c.1558G>T
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XP_011537079.1:p.Ala520Ser
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XM_011538778.1:c.1543G>T
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XP_011537080.1:p.Ala515Ser
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XM_011538779.1:c.1459G>T
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XP_011537081.1:p.Ala487Ser
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XM_011538780.1:c.1444G>T
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XP_011537082.1:p.Ala482Ser
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XM_011538781.1:c.892G>T
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XP_011537083.1:p.Ala298Ser
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XM_011538778.2:c.1543G>T
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XP_011537080.1:p.Ala515Ser
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XM_011538780.2:c.1444G>T
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XP_011537082.1:p.Ala482Ser
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XR_001748875.2:n.1558G>T
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NM_015665.6:c.1501G>T
MANE Select
|
NP_056480.1:p.Ala501Ser
|
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NM_001173466.2:c.1402G>T
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NP_001166937.1:p.Ala468Ser
|
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