ENST00000461280.2:n.1901G>A
|
|
|
ENST00000684241.1:n.3231+205G>A
|
|
|
ENST00000262186.10:c.2398+205G>A
MANE Select
|
ENSP00000262186.5:n.2398+205G>A
|
|
ENST00000330883.9:c.1378+205G>A
|
ENSP00000328531.4:n.1378+205G>A
|
|
ENST00000262186.9:c.2398+205G>A
|
ENSP00000262186.5:n.2398+205G>A
|
|
ENST00000330883.8:c.1378+205G>A
|
ENSP00000328531.4:n.1378+205G>A
|
|
ENST00000430723.4:c.2255G>A
|
ENSP00000387657.4:p.Gly752Asp
|
|
ENST00000461280.1:n.1890G>A
|
|
|
ENST00000473610.5:n.2235G>A
|
|
|
ENST00000532957.5:n.2826G>A
|
|
|
NM_000238.3:c.2398+205G>A , LRG_288t1:c.2398+205G>A
|
NP_000229.1:n.2398+205G>A
|
|
NM_001204798.1:c.1583G>A
|
NP_001191727.1:p.Gly528Asp
|
|
NM_172056.2:c.2603G>A , LRG_288t2:c.2603G>A
|
NP_742053.1:p.Gly868Asp
|
|
NM_172057.2:c.1378+205G>A , LRG_288t3:c.1378+205G>A
|
NP_742054.1:n.1378+205G>A
|
|
XM_011516185.1:c.2098+205G>A
|
XP_011514487.1:n.2098+205G>A
|
|
XM_011516186.1:c.2398+205G>A
|
XP_011514488.1:n.2398+205G>A
|
|
XM_011516185.2:c.2098+205G>A
|
XP_011514487.1:n.2098+205G>A
|
|
XM_011516186.3:c.2398+205G>A
|
XP_011514488.1:n.2398+205G>A
|
|
XM_017012195.1:c.2248+205G>A
|
XP_016867684.1:n.2248+205G>A
|
|
XM_017012196.1:c.2221+205G>A
|
XP_016867685.1:n.2221+205G>A
|
|
NM_000238.4:c.2398+205G>A
MANE Select
|
NP_000229.1:n.2398+205G>A
|
|
NM_001204798.2:c.1583G>A
|
NP_001191727.1:p.Gly528Asp
|
|
NM_172057.3:c.1378+205G>A
|
NP_742054.1:n.1378+205G>A
|
|