|
ENST00000461280.2:n.1209G>C
|
|
|
|
ENST00000683359.1:n.35G>C
|
|
|
|
ENST00000684241.1:n.2744G>C
|
|
|
|
ENST00000262186.10:c.1911G>C
MANE Select
|
ENSP00000262186.5:p.Glu637Asp
|
|
|
ENST00000330883.9:c.891G>C
|
ENSP00000328531.4:p.Glu297Asp
|
|
|
ENST00000262186.9:c.1911G>C
|
ENSP00000262186.5:p.Glu637Asp
|
|
|
ENST00000330883.8:c.891G>C
|
ENSP00000328531.4:p.Glu297Asp
|
|
|
ENST00000430723.4:c.1563G>C
|
ENSP00000387657.4:p.Glu521Asp
|
|
|
ENST00000461280.1:n.1198G>C
|
|
|
|
ENST00000473610.5:n.1216G>C
|
|
|
|
ENST00000532957.5:n.2134G>C
|
|
|
|
NM_000238.3:c.1911G>C , LRG_288t1:c.1911G>C
|
NP_000229.1:p.Glu637Asp
|
|
|
NM_001204798.1:c.891G>C
|
NP_001191727.1:p.Glu297Asp
|
|
|
NM_172056.2:c.1911G>C , LRG_288t2:c.1911G>C
|
NP_742053.1:p.Glu637Asp
|
|
|
NM_172057.2:c.891G>C , LRG_288t3:c.891G>C
|
NP_742054.1:p.Glu297Asp
|
|
|
XM_011516185.1:c.1611G>C
|
XP_011514487.1:p.Glu537Asp
|
|
|
XM_011516186.1:c.1911G>C
|
XP_011514488.1:p.Glu637Asp
|
|
|
XM_011516185.2:c.1611G>C
|
XP_011514487.1:p.Glu537Asp
|
|
|
XM_011516186.3:c.1911G>C
|
XP_011514488.1:p.Glu637Asp
|
|
|
XM_017012195.1:c.1761G>C
|
XP_016867684.1:p.Glu587Asp
|
|
|
XM_017012196.1:c.1734G>C
|
XP_016867685.1:p.Glu578Asp
|
|
|
NM_000238.4:c.1911G>C
MANE Select
|
NP_000229.1:p.Glu637Asp
|
|
|
NM_001204798.2:c.891G>C
|
NP_001191727.1:p.Glu297Asp
|
|
|
NM_172057.3:c.891G>C
|
NP_742054.1:p.Glu297Asp
|
|
