ENST00000461280.2:n.1955C>G
|
|
|
ENST00000684241.1:n.3231+259C>G
|
|
|
ENST00000262186.10:c.2398+259C>G
MANE Select
|
ENSP00000262186.5:n.2398+259C>G
|
|
ENST00000330883.9:c.1378+259C>G
|
ENSP00000328531.4:n.1378+259C>G
|
|
ENST00000262186.9:c.2398+259C>G
|
ENSP00000262186.5:n.2398+259C>G
|
|
ENST00000330883.8:c.1378+259C>G
|
ENSP00000328531.4:n.1378+259C>G
|
|
ENST00000430723.4:c.2309C>G
|
ENSP00000387657.4:p.Ser770Cys
|
|
ENST00000461280.1:n.1944C>G
|
|
|
ENST00000473610.5:n.2289C>G
|
|
|
ENST00000532957.5:n.2880C>G
|
|
|
NM_000238.3:c.2398+259C>G , LRG_288t1:c.2398+259C>G
|
NP_000229.1:n.2398+259C>G
|
|
NM_001204798.1:c.1637C>G
|
NP_001191727.1:p.Ser546Cys
|
|
NM_172056.2:c.2657C>G , LRG_288t2:c.2657C>G
|
NP_742053.1:p.Ser886Cys
|
|
NM_172057.2:c.1378+259C>G , LRG_288t3:c.1378+259C>G
|
NP_742054.1:n.1378+259C>G
|
|
XM_011516185.1:c.2098+259C>G
|
XP_011514487.1:n.2098+259C>G
|
|
XM_011516186.1:c.2398+259C>G
|
XP_011514488.1:n.2398+259C>G
|
|
XM_011516185.2:c.2098+259C>G
|
XP_011514487.1:n.2098+259C>G
|
|
XM_011516186.3:c.2398+259C>G
|
XP_011514488.1:n.2398+259C>G
|
|
XM_017012195.1:c.2248+259C>G
|
XP_016867684.1:n.2248+259C>G
|
|
XM_017012196.1:c.2221+259C>G
|
XP_016867685.1:n.2221+259C>G
|
|
NM_000238.4:c.2398+259C>G
MANE Select
|
NP_000229.1:n.2398+259C>G
|
|
NM_001204798.2:c.1637C>G
|
NP_001191727.1:p.Ser546Cys
|
|
NM_172057.3:c.1378+259C>G
|
NP_742054.1:n.1378+259C>G
|
|