ENST00000461280.2:n.1483T>G
|
|
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ENST00000684241.1:n.3018T>G
|
|
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ENST00000262186.10:c.2185T>G
MANE Select
|
ENSP00000262186.5:p.Cys729Gly
|
|
ENST00000330883.9:c.1165T>G
|
ENSP00000328531.4:p.Cys389Gly
|
|
ENST00000262186.9:c.2185T>G
|
ENSP00000262186.5:p.Cys729Gly
|
|
ENST00000330883.8:c.1165T>G
|
ENSP00000328531.4:p.Cys389Gly
|
|
ENST00000430723.4:c.1837T>G
|
ENSP00000387657.4:p.Cys613Gly
|
|
ENST00000461280.1:n.1472T>G
|
|
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ENST00000473610.5:n.1817T>G
|
|
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ENST00000532957.5:n.2408T>G
|
|
|
NM_000238.3:c.2185T>G , LRG_288t1:c.2185T>G
|
NP_000229.1:p.Cys729Gly
|
|
NM_001204798.1:c.1165T>G
|
NP_001191727.1:p.Cys389Gly
|
|
NM_172056.2:c.2185T>G , LRG_288t2:c.2185T>G
|
NP_742053.1:p.Cys729Gly
|
|
NM_172057.2:c.1165T>G , LRG_288t3:c.1165T>G
|
NP_742054.1:p.Cys389Gly
|
|
XM_011516185.1:c.1885T>G
|
XP_011514487.1:p.Cys629Gly
|
|
XM_011516186.1:c.2185T>G
|
XP_011514488.1:p.Cys729Gly
|
|
XM_011516185.2:c.1885T>G
|
XP_011514487.1:p.Cys629Gly
|
|
XM_011516186.3:c.2185T>G
|
XP_011514488.1:p.Cys729Gly
|
|
XM_017012195.1:c.2035T>G
|
XP_016867684.1:p.Cys679Gly
|
|
XM_017012196.1:c.2008T>G
|
XP_016867685.1:p.Cys670Gly
|
|
NM_000238.4:c.2185T>G
MANE Select
|
NP_000229.1:p.Cys729Gly
|
|
NM_001204798.2:c.1165T>G
|
NP_001191727.1:p.Cys389Gly
|
|
NM_172057.3:c.1165T>G
|
NP_742054.1:p.Cys389Gly
|
|