ENST00000461280.2:n.1207G>T
|
|
|
ENST00000683359.1:n.33G>T
|
|
|
ENST00000684241.1:n.2742G>T
|
|
|
ENST00000262186.10:c.1909G>T
MANE Select
|
ENSP00000262186.5:p.Glu637Ter
|
|
ENST00000330883.9:c.889G>T
|
ENSP00000328531.4:p.Glu297Ter
|
|
ENST00000262186.9:c.1909G>T
|
ENSP00000262186.5:p.Glu637Ter
|
|
ENST00000330883.8:c.889G>T
|
ENSP00000328531.4:p.Glu297Ter
|
|
ENST00000430723.4:c.1561G>T
|
ENSP00000387657.4:p.Glu521Ter
|
|
ENST00000461280.1:n.1196G>T
|
|
|
ENST00000473610.5:n.1214G>T
|
|
|
ENST00000532957.5:n.2132G>T
|
|
|
NM_000238.3:c.1909G>T , LRG_288t1:c.1909G>T
|
NP_000229.1:p.Glu637Ter
|
|
NM_001204798.1:c.889G>T
|
NP_001191727.1:p.Glu297Ter
|
|
NM_172056.2:c.1909G>T , LRG_288t2:c.1909G>T
|
NP_742053.1:p.Glu637Ter
|
|
NM_172057.2:c.889G>T , LRG_288t3:c.889G>T
|
NP_742054.1:p.Glu297Ter
|
|
XM_011516185.1:c.1609G>T
|
XP_011514487.1:p.Glu537Ter
|
|
XM_011516186.1:c.1909G>T
|
XP_011514488.1:p.Glu637Ter
|
|
XM_011516185.2:c.1609G>T
|
XP_011514487.1:p.Glu537Ter
|
|
XM_011516186.3:c.1909G>T
|
XP_011514488.1:p.Glu637Ter
|
|
XM_017012195.1:c.1759G>T
|
XP_016867684.1:p.Glu587Ter
|
|
XM_017012196.1:c.1732G>T
|
XP_016867685.1:p.Glu578Ter
|
|
NM_000238.4:c.1909G>T
MANE Select
|
NP_000229.1:p.Glu637Ter
|
|
NM_001204798.2:c.889G>T
|
NP_001191727.1:p.Glu297Ter
|
|
NM_172057.3:c.889G>T
|
NP_742054.1:p.Glu297Ter
|
|