ENST00000686218.1:c.-677G>T
|
ENSP00000509288.1:n.-677G>T
|
|
ENST00000691249.1:n.73G>T
|
|
|
ENST00000442944.7:c.33+229G>T
|
ENSP00000392041.3:n.33+229G>T
|
|
ENST00000534956.2:n.36+229G>T
|
|
|
ENST00000536813.6:c.-102+229G>T
|
ENSP00000438726.2:n.-102+229G>T
|
|
ENST00000546302.6:c.33+229G>T
|
ENSP00000445599.1:n.33+229G>T
|
|
ENST00000640813.1:c.-19+229G>T
|
ENSP00000491061.1:n.-19+229G>T
|
|
ENST00000648026.1:c.27+229G>T
|
ENSP00000498044.1:n.27+229G>T
|
|
ENST00000649823.1:n.6G>T
|
|
|
ENST00000649868.1:c.33+229G>T
|
ENSP00000497548.1:n.33+229G>T
|
|
ENST00000650101.1:c.-617G>T
|
ENSP00000496970.1:n.-617G>T
|
|
ENST00000650307.1:n.52G>T
|
|
|
ENST00000652429.1:c.33+229G>T
MANE Select
|
ENSP00000498786.1:n.33+229G>T
|
|
ENST00000278715.7:c.33+229G>T
|
ENSP00000278715.3:n.33+229G>T
|
|
ENST00000442944.6:c.-102+229G>T
|
ENSP00000392041.2:n.-102+229G>T
|
|
ENST00000535793.5:c.33+229G>T
|
ENSP00000439904.1:n.33+229G>T
|
|
ENST00000536185.5:n.201+229G>T
|
|
|
ENST00000536813.5:c.33+229G>T
|
ENSP00000438726.1:n.33+229G>T
|
|
ENST00000537841.5:c.-19+138G>T
|
ENSP00000444730.1:n.-19+138G>T
|
|
ENST00000542044.5:n.158+229G>T
|
|
|
ENST00000542729.5:c.-19+138G>T
|
ENSP00000443058.1:n.-19+138G>T
|
|
ENST00000542822.5:c.124+138G>T
|
ENSP00000444817.1:n.124+138G>T
|
|
ENST00000543090.5:c.33+229G>T
|
ENSP00000445429.1:n.33+229G>T
|
|
ENST00000543821.5:n.179+229G>T
|
|
|
ENST00000544387.5:c.33+229G>T
|
ENSP00000438424.1:n.33+229G>T
|
|
ENST00000545621.5:c.33+229G>T
|
ENSP00000444849.1:n.33+229G>T
|
|
ENST00000545901.5:n.186+229G>T
|
|
|
ENST00000546302.5:c.33+229G>T
|
ENSP00000445599.1:n.33+229G>T
|
|
NM_000190.3:c.33+229G>T
|
NP_000181.2:n.33+229G>T
|
|
NM_001258208.1:c.33+229G>T
|
NP_001245137.1:n.33+229G>T
|
|
NM_001258209.1:c.-19+138G>T
|
NP_001245138.1:n.-19+138G>T
|
|
XM_005271531.1:c.-19+138G>T
|
XP_005271588.1:n.-19+138G>T
|
|
XM_005271532.1:c.-19+162G>T
|
XP_005271589.1:n.-19+162G>T
|
|
XM_005271533.2:c.33+229G>T
|
XP_005271590.1:n.33+229G>T
|
|
NM_000190.4:c.33+229G>T
MANE Select
|
NP_000181.2:n.33+229G>T
|
|
XM_005271533.3:c.33+229G>T
|
XP_005271590.1:n.33+229G>T
|
|
XM_024448460.1:c.33+229G>T
|
XP_024304228.1:n.33+229G>T
|
|
NM_001258208.2:c.33+229G>T
|
NP_001245137.1:n.33+229G>T
|
|
NM_001258209.2:c.-19+138G>T
|
NP_001245138.1:n.-19+138G>T
|
|