ENST00000461280.2:n.1673G>T
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|
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ENST00000684241.1:n.3208G>T
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|
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ENST00000262186.10:c.2375G>T
MANE Select
|
ENSP00000262186.5:p.Gly792Val
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ENST00000330883.9:c.1355G>T
|
ENSP00000328531.4:p.Gly452Val
|
|
ENST00000262186.9:c.2375G>T
|
ENSP00000262186.5:p.Gly792Val
|
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ENST00000330883.8:c.1355G>T
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ENSP00000328531.4:p.Gly452Val
|
|
ENST00000430723.4:c.2027G>T
|
ENSP00000387657.4:p.Gly676Val
|
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ENST00000461280.1:n.1662G>T
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|
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ENST00000473610.5:n.2007G>T
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|
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ENST00000532957.5:n.2598G>T
|
|
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NM_000238.3:c.2375G>T , LRG_288t1:c.2375G>T
|
NP_000229.1:p.Gly792Val
|
|
NM_001204798.1:c.1355G>T
|
NP_001191727.1:p.Gly452Val
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NM_172056.2:c.2375G>T , LRG_288t2:c.2375G>T
|
NP_742053.1:p.Gly792Val
|
|
NM_172057.2:c.1355G>T , LRG_288t3:c.1355G>T
|
NP_742054.1:p.Gly452Val
|
|
XM_011516185.1:c.2075G>T
|
XP_011514487.1:p.Gly692Val
|
|
XM_011516186.1:c.2375G>T
|
XP_011514488.1:p.Gly792Val
|
|
XM_011516185.2:c.2075G>T
|
XP_011514487.1:p.Gly692Val
|
|
XM_011516186.3:c.2375G>T
|
XP_011514488.1:p.Gly792Val
|
|
XM_017012195.1:c.2225G>T
|
XP_016867684.1:p.Gly742Val
|
|
XM_017012196.1:c.2198G>T
|
XP_016867685.1:p.Gly733Val
|
|
NM_000238.4:c.2375G>T
MANE Select
|
NP_000229.1:p.Gly792Val
|
|
NM_001204798.2:c.1355G>T
|
NP_001191727.1:p.Gly452Val
|
|
NM_172057.3:c.1355G>T
|
NP_742054.1:p.Gly452Val
|
|