ENST00000461280.2:n.428T>A
|
|
|
ENST00000684116.1:n.23T>A
|
|
|
ENST00000684241.1:n.1963T>A
|
|
|
ENST00000262186.10:c.1130T>A
MANE Select
|
ENSP00000262186.5:p.Val377Asp
|
|
ENST00000330883.9:c.110T>A
|
ENSP00000328531.4:p.Val37Asp
|
|
ENST00000262186.9:c.1130T>A
|
ENSP00000262186.5:p.Val377Asp
|
|
ENST00000330883.8:c.110T>A
|
ENSP00000328531.4:p.Val37Asp
|
|
ENST00000430723.4:c.782T>A
|
ENSP00000387657.4:p.Val261Asp
|
|
ENST00000461280.1:n.417T>A
|
|
|
ENST00000473610.5:n.435T>A
|
|
|
ENST00000532957.5:n.1353T>A
|
|
|
NM_000238.3:c.1130T>A , LRG_288t1:c.1130T>A
|
NP_000229.1:p.Val377Asp
|
|
NM_001204798.1:c.110T>A
|
NP_001191727.1:p.Val37Asp
|
|
NM_172056.2:c.1130T>A , LRG_288t2:c.1130T>A
|
NP_742053.1:p.Val377Asp
|
|
NM_172057.2:c.110T>A , LRG_288t3:c.110T>A
|
NP_742054.1:p.Val37Asp
|
|
XM_011516185.1:c.830T>A
|
XP_011514487.1:p.Val277Asp
|
|
XM_011516186.1:c.1130T>A
|
XP_011514488.1:p.Val377Asp
|
|
XM_011516185.2:c.830T>A
|
XP_011514487.1:p.Val277Asp
|
|
XM_011516186.3:c.1130T>A
|
XP_011514488.1:p.Val377Asp
|
|
XM_017012195.1:c.980T>A
|
XP_016867684.1:p.Val327Asp
|
|
XM_017012196.1:c.953T>A
|
XP_016867685.1:p.Val318Asp
|
|
NM_000238.4:c.1130T>A
MANE Select
|
NP_000229.1:p.Val377Asp
|
|
NM_001204798.2:c.110T>A
|
NP_001191727.1:p.Val37Asp
|
|
NM_172057.3:c.110T>A
|
NP_742054.1:p.Val37Asp
|
|