ENST00000209873.9:c.1576G>T
MANE Select
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ENSP00000209873.4:p.Ala526Ser
|
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ENST00000546562.6:n.2640G>T
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|
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ENST00000547238.6:n.2212G>T
|
|
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ENST00000547520.6:n.1692G>T
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|
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ENST00000547757.2:c.*494G>T
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ENSP00000448020.2:n.*494G>T
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ENST00000548931.6:c.1011G>T
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ENSP00000457518.1:p.Leu337=
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ENST00000549450.6:n.1510G>T
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|
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ENST00000672797.1:n.2065G>T
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|
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ENST00000209873.8:c.1576G>T
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ENSP00000209873.4:p.Ala526Ser
|
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ENST00000394384.7:c.1477G>T
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ENSP00000377908.3:p.Ala493Ser
|
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ENST00000548931.5:c.1011G>T
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ENSP00000457518.1:p.Leu337=
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ENST00000550286.5:c.1204G>T
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ENSP00000446885.1:p.Ala402Ser
|
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ENST00000552876.5:n.1919G>T
|
|
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NM_001173466.1:c.1477G>T
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NP_001166937.1:p.Ala493Ser
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|
NM_015665.5:c.1576G>T
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NP_056480.1:p.Ala526Ser
|
|
XM_006719617.2:c.1591G>T
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XP_006719680.1:p.Ala531Ser
|
|
XM_011538777.1:c.1633G>T
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XP_011537079.1:p.Ala545Ser
|
|
XM_011538778.1:c.1618G>T
|
XP_011537080.1:p.Ala540Ser
|
|
XM_011538779.1:c.1534G>T
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XP_011537081.1:p.Ala512Ser
|
|
XM_011538780.1:c.1519G>T
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XP_011537082.1:p.Ala507Ser
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XM_011538781.1:c.967G>T
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XP_011537083.1:p.Ala323Ser
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|
XM_011538778.2:c.1618G>T
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XP_011537080.1:p.Ala540Ser
|
|
XM_011538780.2:c.1519G>T
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XP_011537082.1:p.Ala507Ser
|
|
XR_001748875.2:n.1633G>T
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|
|
NM_015665.6:c.1576G>T
MANE Select
|
NP_056480.1:p.Ala526Ser
|
|
NM_001173466.2:c.1477G>T
|
NP_001166937.1:p.Ala493Ser
|
|