ENST00000461280.2:n.1738G>A
|
|
|
ENST00000684241.1:n.3231+42G>A
|
|
|
ENST00000262186.10:c.2398+42G>A
MANE Select
|
ENSP00000262186.5:n.2398+42G>A
|
|
ENST00000330883.9:c.1378+42G>A
|
ENSP00000328531.4:n.1378+42G>A
|
|
ENST00000262186.9:c.2398+42G>A
|
ENSP00000262186.5:n.2398+42G>A
|
|
ENST00000330883.8:c.1378+42G>A
|
ENSP00000328531.4:n.1378+42G>A
|
|
ENST00000430723.4:c.2092G>A
|
ENSP00000387657.4:p.Ala698Thr
|
|
ENST00000461280.1:n.1727G>A
|
|
|
ENST00000473610.5:n.2072G>A
|
|
|
ENST00000532957.5:n.2663G>A
|
|
|
NM_000238.3:c.2398+42G>A , LRG_288t1:c.2398+42G>A
|
NP_000229.1:n.2398+42G>A
|
|
NM_001204798.1:c.1420G>A
|
NP_001191727.1:p.Ala474Thr
|
|
NM_172056.2:c.2440G>A , LRG_288t2:c.2440G>A
|
NP_742053.1:p.Ala814Thr
|
|
NM_172057.2:c.1378+42G>A , LRG_288t3:c.1378+42G>A
|
NP_742054.1:n.1378+42G>A
|
|
XM_011516185.1:c.2098+42G>A
|
XP_011514487.1:n.2098+42G>A
|
|
XM_011516186.1:c.2398+42G>A
|
XP_011514488.1:n.2398+42G>A
|
|
XM_011516185.2:c.2098+42G>A
|
XP_011514487.1:n.2098+42G>A
|
|
XM_011516186.3:c.2398+42G>A
|
XP_011514488.1:n.2398+42G>A
|
|
XM_017012195.1:c.2248+42G>A
|
XP_016867684.1:n.2248+42G>A
|
|
XM_017012196.1:c.2221+42G>A
|
XP_016867685.1:n.2221+42G>A
|
|
NM_000238.4:c.2398+42G>A
MANE Select
|
NP_000229.1:n.2398+42G>A
|
|
NM_001204798.2:c.1420G>A
|
NP_001191727.1:p.Ala474Thr
|
|
NM_172057.3:c.1378+42G>A
|
NP_742054.1:n.1378+42G>A
|
|