ENST00000461280.2:n.1672G>T
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|
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ENST00000684241.1:n.3207G>T
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|
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ENST00000262186.10:c.2374G>T
MANE Select
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ENSP00000262186.5:p.Gly792Cys
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ENST00000330883.9:c.1354G>T
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ENSP00000328531.4:p.Gly452Cys
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ENST00000262186.9:c.2374G>T
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ENSP00000262186.5:p.Gly792Cys
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ENST00000330883.8:c.1354G>T
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ENSP00000328531.4:p.Gly452Cys
|
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ENST00000430723.4:c.2026G>T
|
ENSP00000387657.4:p.Gly676Cys
|
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ENST00000461280.1:n.1661G>T
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|
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ENST00000473610.5:n.2006G>T
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|
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ENST00000532957.5:n.2597G>T
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NM_000238.3:c.2374G>T , LRG_288t1:c.2374G>T
|
NP_000229.1:p.Gly792Cys
|
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NM_001204798.1:c.1354G>T
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NP_001191727.1:p.Gly452Cys
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NM_172056.2:c.2374G>T , LRG_288t2:c.2374G>T
|
NP_742053.1:p.Gly792Cys
|
|
NM_172057.2:c.1354G>T , LRG_288t3:c.1354G>T
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NP_742054.1:p.Gly452Cys
|
|
XM_011516185.1:c.2074G>T
|
XP_011514487.1:p.Gly692Cys
|
|
XM_011516186.1:c.2374G>T
|
XP_011514488.1:p.Gly792Cys
|
|
XM_011516185.2:c.2074G>T
|
XP_011514487.1:p.Gly692Cys
|
|
XM_011516186.3:c.2374G>T
|
XP_011514488.1:p.Gly792Cys
|
|
XM_017012195.1:c.2224G>T
|
XP_016867684.1:p.Gly742Cys
|
|
XM_017012196.1:c.2197G>T
|
XP_016867685.1:p.Gly733Cys
|
|
NM_000238.4:c.2374G>T
MANE Select
|
NP_000229.1:p.Gly792Cys
|
|
NM_001204798.2:c.1354G>T
|
NP_001191727.1:p.Gly452Cys
|
|
NM_172057.3:c.1354G>T
|
NP_742054.1:p.Gly452Cys
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