ENST00000461280.2:n.1707G>T
|
|
|
ENST00000684241.1:n.3231+11G>T
|
|
|
ENST00000262186.10:c.2398+11G>T
MANE Select
|
ENSP00000262186.5:n.2398+11G>T
|
|
ENST00000330883.9:c.1378+11G>T
|
ENSP00000328531.4:n.1378+11G>T
|
|
ENST00000262186.9:c.2398+11G>T
|
ENSP00000262186.5:n.2398+11G>T
|
|
ENST00000330883.8:c.1378+11G>T
|
ENSP00000328531.4:n.1378+11G>T
|
|
ENST00000430723.4:c.2061G>T
|
ENSP00000387657.4:p.Trp687Cys
|
|
ENST00000461280.1:n.1696G>T
|
|
|
ENST00000473610.5:n.2041G>T
|
|
|
ENST00000532957.5:n.2632G>T
|
|
|
NM_000238.3:c.2398+11G>T , LRG_288t1:c.2398+11G>T
|
NP_000229.1:n.2398+11G>T
|
|
NM_001204798.1:c.1389G>T
|
NP_001191727.1:p.Trp463Cys
|
|
NM_172056.2:c.2409G>T , LRG_288t2:c.2409G>T
|
NP_742053.1:p.Trp803Cys
|
|
NM_172057.2:c.1378+11G>T , LRG_288t3:c.1378+11G>T
|
NP_742054.1:n.1378+11G>T
|
|
XM_011516185.1:c.2098+11G>T
|
XP_011514487.1:n.2098+11G>T
|
|
XM_011516186.1:c.2398+11G>T
|
XP_011514488.1:n.2398+11G>T
|
|
XM_011516185.2:c.2098+11G>T
|
XP_011514487.1:n.2098+11G>T
|
|
XM_011516186.3:c.2398+11G>T
|
XP_011514488.1:n.2398+11G>T
|
|
XM_017012195.1:c.2248+11G>T
|
XP_016867684.1:n.2248+11G>T
|
|
XM_017012196.1:c.2221+11G>T
|
XP_016867685.1:n.2221+11G>T
|
|
NM_000238.4:c.2398+11G>T
MANE Select
|
NP_000229.1:n.2398+11G>T
|
|
NM_001204798.2:c.1389G>T
|
NP_001191727.1:p.Trp463Cys
|
|
NM_172057.3:c.1378+11G>T
|
NP_742054.1:n.1378+11G>T
|
|