ENST00000461280.2:n.1309G>T
|
|
|
ENST00000683359.1:n.135G>T
|
|
|
ENST00000684241.1:n.2844G>T
|
|
|
ENST00000262186.10:c.2011G>T
MANE Select
|
ENSP00000262186.5:p.Ala671Ser
|
|
ENST00000330883.9:c.991G>T
|
ENSP00000328531.4:p.Ala331Ser
|
|
ENST00000262186.9:c.2011G>T
|
ENSP00000262186.5:p.Ala671Ser
|
|
ENST00000330883.8:c.991G>T
|
ENSP00000328531.4:p.Ala331Ser
|
|
ENST00000430723.4:c.1663G>T
|
ENSP00000387657.4:p.Ala555Ser
|
|
ENST00000461280.1:n.1298G>T
|
|
|
ENST00000473610.5:n.1643G>T
|
|
|
ENST00000532957.5:n.2234G>T
|
|
|
NM_000238.3:c.2011G>T , LRG_288t1:c.2011G>T
|
NP_000229.1:p.Ala671Ser
|
|
NM_001204798.1:c.991G>T
|
NP_001191727.1:p.Ala331Ser
|
|
NM_172056.2:c.2011G>T , LRG_288t2:c.2011G>T
|
NP_742053.1:p.Ala671Ser
|
|
NM_172057.2:c.991G>T , LRG_288t3:c.991G>T
|
NP_742054.1:p.Ala331Ser
|
|
XM_011516185.1:c.1711G>T
|
XP_011514487.1:p.Ala571Ser
|
|
XM_011516186.1:c.2011G>T
|
XP_011514488.1:p.Ala671Ser
|
|
XM_011516185.2:c.1711G>T
|
XP_011514487.1:p.Ala571Ser
|
|
XM_011516186.3:c.2011G>T
|
XP_011514488.1:p.Ala671Ser
|
|
XM_017012195.1:c.1861G>T
|
XP_016867684.1:p.Ala621Ser
|
|
XM_017012196.1:c.1834G>T
|
XP_016867685.1:p.Ala612Ser
|
|
NM_000238.4:c.2011G>T
MANE Select
|
NP_000229.1:p.Ala671Ser
|
|
NM_001204798.2:c.991G>T
|
NP_001191727.1:p.Ala331Ser
|
|
NM_172057.3:c.991G>T
|
NP_742054.1:p.Ala331Ser
|
|