ENST00000461280.2:n.182G>T
|
|
|
ENST00000684241.1:n.1961+1651G>T
|
|
|
ENST00000262186.10:c.1128+1651G>T
MANE Select
|
ENSP00000262186.5:n.1128+1651G>T
|
|
ENST00000330883.9:c.-137G>T
|
ENSP00000328531.4:n.-137G>T
|
|
ENST00000262186.9:c.1128+1651G>T
|
ENSP00000262186.5:n.1128+1651G>T
|
|
ENST00000330883.8:c.-137G>T
|
ENSP00000328531.4:n.-137G>T
|
|
ENST00000430723.4:c.780+1651G>T
|
ENSP00000387657.4:n.780+1651G>T
|
|
ENST00000461280.1:n.171G>T
|
|
|
ENST00000473610.5:n.189G>T
|
|
|
ENST00000532957.5:n.1351+1651G>T
|
|
|
NM_000238.3:c.1128+1651G>T , LRG_288t1:c.1128+1651G>T
|
NP_000229.1:n.1128+1651G>T
|
|
NM_001204798.1:c.-137G>T
|
NP_001191727.1:n.-137G>T
|
|
NM_172056.2:c.1128+1651G>T , LRG_288t2:c.1128+1651G>T
|
NP_742053.1:n.1128+1651G>T
|
|
NM_172057.2:c.-137G>T , LRG_288t3:c.-137G>T
|
NP_742054.1:n.-137G>T
|
|
XM_011516185.1:c.828+1651G>T
|
XP_011514487.1:n.828+1651G>T
|
|
XM_011516186.1:c.1128+1651G>T
|
XP_011514488.1:n.1128+1651G>T
|
|
XM_011516185.2:c.828+1651G>T
|
XP_011514487.1:n.828+1651G>T
|
|
XM_011516186.3:c.1128+1651G>T
|
XP_011514488.1:n.1128+1651G>T
|
|
XM_017012195.1:c.978+1651G>T
|
XP_016867684.1:n.978+1651G>T
|
|
XM_017012196.1:c.951+1651G>T
|
XP_016867685.1:n.951+1651G>T
|
|
NM_000238.4:c.1128+1651G>T
MANE Select
|
NP_000229.1:n.1128+1651G>T
|
|
NM_001204798.2:c.-137G>T
|
NP_001191727.1:n.-137G>T
|
|
NM_172057.3:c.-137G>T
|
NP_742054.1:n.-137G>T
|
|