ENST00000684241.1:n.1774G>T
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ENST00000262186.10:c.941G>T
MANE Select
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ENSP00000262186.5:p.Gly314Val
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ENST00000262186.9:c.941G>T
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ENSP00000262186.5:p.Gly314Val
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|
ENST00000430723.4:c.593G>T
|
ENSP00000387657.4:p.Gly198Val
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ENST00000532957.5:n.1164G>T
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NM_000238.3:c.941G>T , LRG_288t1:c.941G>T
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NP_000229.1:p.Gly314Val
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NM_172056.2:c.941G>T , LRG_288t2:c.941G>T
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NP_742053.1:p.Gly314Val
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XM_011516185.1:c.641G>T
|
XP_011514487.1:p.Gly214Val
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XM_011516186.1:c.941G>T
|
XP_011514488.1:p.Gly314Val
|
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XM_011516185.2:c.641G>T
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XP_011514487.1:p.Gly214Val
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XM_011516186.3:c.941G>T
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XP_011514488.1:p.Gly314Val
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XM_017012195.1:c.791G>T
|
XP_016867684.1:p.Gly264Val
|
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XM_017012196.1:c.764G>T
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XP_016867685.1:p.Gly255Val
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NM_000238.4:c.941G>T
MANE Select
|
NP_000229.1:p.Gly314Val
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