ENST00000461280.2:n.1725G>C
|
|
|
ENST00000684241.1:n.3231+29G>C
|
|
|
ENST00000262186.10:c.2398+29G>C
MANE Select
|
ENSP00000262186.5:n.2398+29G>C
|
|
ENST00000330883.9:c.1378+29G>C
|
ENSP00000328531.4:n.1378+29G>C
|
|
ENST00000262186.9:c.2398+29G>C
|
ENSP00000262186.5:n.2398+29G>C
|
|
ENST00000330883.8:c.1378+29G>C
|
ENSP00000328531.4:n.1378+29G>C
|
|
ENST00000430723.4:c.2079G>C
|
ENSP00000387657.4:p.Leu693=
|
|
ENST00000461280.1:n.1714G>C
|
|
|
ENST00000473610.5:n.2059G>C
|
|
|
ENST00000532957.5:n.2650G>C
|
|
|
NM_000238.3:c.2398+29G>C , LRG_288t1:c.2398+29G>C
|
NP_000229.1:n.2398+29G>C
|
|
NM_001204798.1:c.1407G>C
|
NP_001191727.1:p.Leu469=
|
|
NM_172056.2:c.2427G>C , LRG_288t2:c.2427G>C
|
NP_742053.1:p.Leu809=
|
|
NM_172057.2:c.1378+29G>C , LRG_288t3:c.1378+29G>C
|
NP_742054.1:n.1378+29G>C
|
|
XM_011516185.1:c.2098+29G>C
|
XP_011514487.1:n.2098+29G>C
|
|
XM_011516186.1:c.2398+29G>C
|
XP_011514488.1:n.2398+29G>C
|
|
XM_011516185.2:c.2098+29G>C
|
XP_011514487.1:n.2098+29G>C
|
|
XM_011516186.3:c.2398+29G>C
|
XP_011514488.1:n.2398+29G>C
|
|
XM_017012195.1:c.2248+29G>C
|
XP_016867684.1:n.2248+29G>C
|
|
XM_017012196.1:c.2221+29G>C
|
XP_016867685.1:n.2221+29G>C
|
|
NM_000238.4:c.2398+29G>C
MANE Select
|
NP_000229.1:n.2398+29G>C
|
|
NM_001204798.2:c.1407G>C
|
NP_001191727.1:p.Leu469=
|
|
NM_172057.3:c.1378+29G>C
|
NP_742054.1:n.1378+29G>C
|
|