ENST00000461280.2:n.1563C>T
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|
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ENST00000684241.1:n.3098C>T
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|
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ENST00000262186.10:c.2265C>T
MANE Select
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ENSP00000262186.5:p.Ala755=
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ENST00000330883.9:c.1245C>T
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ENSP00000328531.4:p.Ala415=
|
|
ENST00000262186.9:c.2265C>T
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ENSP00000262186.5:p.Ala755=
|
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ENST00000330883.8:c.1245C>T
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ENSP00000328531.4:p.Ala415=
|
|
ENST00000430723.4:c.1917C>T
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ENSP00000387657.4:p.Ala639=
|
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ENST00000461280.1:n.1552C>T
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ENST00000473610.5:n.1897C>T
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|
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ENST00000532957.5:n.2488C>T
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|
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NM_000238.3:c.2265C>T , LRG_288t1:c.2265C>T
|
NP_000229.1:p.Ala755=
|
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NM_001204798.1:c.1245C>T
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NP_001191727.1:p.Ala415=
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NM_172056.2:c.2265C>T , LRG_288t2:c.2265C>T
|
NP_742053.1:p.Ala755=
|
|
NM_172057.2:c.1245C>T , LRG_288t3:c.1245C>T
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NP_742054.1:p.Ala415=
|
|
XM_011516185.1:c.1965C>T
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XP_011514487.1:p.Ala655=
|
|
XM_011516186.1:c.2265C>T
|
XP_011514488.1:p.Ala755=
|
|
XM_011516185.2:c.1965C>T
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XP_011514487.1:p.Ala655=
|
|
XM_011516186.3:c.2265C>T
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XP_011514488.1:p.Ala755=
|
|
XM_017012195.1:c.2115C>T
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XP_016867684.1:p.Ala705=
|
|
XM_017012196.1:c.2088C>T
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XP_016867685.1:p.Ala696=
|
|
NM_000238.4:c.2265C>T
MANE Select
|
NP_000229.1:p.Ala755=
|
|
NM_001204798.2:c.1245C>T
|
NP_001191727.1:p.Ala415=
|
|
NM_172057.3:c.1245C>T
|
NP_742054.1:p.Ala415=
|
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