ENST00000461280.2:n.1860G>C
|
|
|
ENST00000684241.1:n.3231+164G>C
|
|
|
ENST00000262186.10:c.2398+164G>C
MANE Select
|
ENSP00000262186.5:n.2398+164G>C
|
|
ENST00000330883.9:c.1378+164G>C
|
ENSP00000328531.4:n.1378+164G>C
|
|
ENST00000262186.9:c.2398+164G>C
|
ENSP00000262186.5:n.2398+164G>C
|
|
ENST00000330883.8:c.1378+164G>C
|
ENSP00000328531.4:n.1378+164G>C
|
|
ENST00000430723.4:c.2214G>C
|
ENSP00000387657.4:p.Met738Ile
|
|
ENST00000461280.1:n.1849G>C
|
|
|
ENST00000473610.5:n.2194G>C
|
|
|
ENST00000532957.5:n.2785G>C
|
|
|
NM_000238.3:c.2398+164G>C , LRG_288t1:c.2398+164G>C
|
NP_000229.1:n.2398+164G>C
|
|
NM_001204798.1:c.1542G>C
|
NP_001191727.1:p.Met514Ile
|
|
NM_172056.2:c.2562G>C , LRG_288t2:c.2562G>C
|
NP_742053.1:p.Met854Ile
|
|
NM_172057.2:c.1378+164G>C , LRG_288t3:c.1378+164G>C
|
NP_742054.1:n.1378+164G>C
|
|
XM_011516185.1:c.2098+164G>C
|
XP_011514487.1:n.2098+164G>C
|
|
XM_011516186.1:c.2398+164G>C
|
XP_011514488.1:n.2398+164G>C
|
|
XM_011516185.2:c.2098+164G>C
|
XP_011514487.1:n.2098+164G>C
|
|
XM_011516186.3:c.2398+164G>C
|
XP_011514488.1:n.2398+164G>C
|
|
XM_017012195.1:c.2248+164G>C
|
XP_016867684.1:n.2248+164G>C
|
|
XM_017012196.1:c.2221+164G>C
|
XP_016867685.1:n.2221+164G>C
|
|
NM_000238.4:c.2398+164G>C
MANE Select
|
NP_000229.1:n.2398+164G>C
|
|
NM_001204798.2:c.1542G>C
|
NP_001191727.1:p.Met514Ile
|
|
NM_172057.3:c.1378+164G>C
|
NP_742054.1:n.1378+164G>C
|
|