ENST00000711048.1:c.1009-589C>G
|
ENSP00000518557.1:n.1009-589C>G
|
|
ENST00000402731.6:c.937C>G
|
ENSP00000384835.2:p.Leu313Val
|
|
ENST00000404276.6:c.1138C>G
MANE Select
|
ENSP00000385747.1:p.Leu380Val
|
|
ENST00000425190.7:c.475C>G
|
ENSP00000390244.2:p.Leu159Val
|
|
ENST00000464581.6:c.478C>G
|
ENSP00000483777.2:p.Leu160Val
|
|
ENST00000648295.1:n.690C>G
|
|
|
ENST00000649563.1:c.475C>G
|
ENSP00000496928.1:p.Leu159Val
|
|
ENST00000650281.1:c.1138C>G
|
ENSP00000497000.1:p.Leu380Val
|
|
ENST00000328354.10:c.1138C>G
|
ENSP00000329178.6:p.Leu380Val
|
|
ENST00000348295.7:c.1051C>G
|
ENSP00000329012.5:p.Leu351Val
|
|
ENST00000382580.6:c.1267C>G
|
ENSP00000372023.2:p.Leu423Val
|
|
ENST00000402731.5:c.1051C>G
|
ENSP00000384835.1:p.Leu351Val
|
|
ENST00000403642.5:c.865C>G
|
ENSP00000384919.1:p.Leu289Val
|
|
ENST00000404276.5:c.1138C>G
|
ENSP00000385747.1:p.Leu380Val
|
|
ENST00000405598.5:c.1138C>G
|
ENSP00000386087.1:p.Leu380Val
|
|
ENST00000416671.5:c.*628C>G
|
ENSP00000402225.1:n.*628C>G
|
|
ENST00000417588.5:c.1047C>G
|
ENSP00000412901.1:n.1047C>G
|
|
ENST00000433728.5:c.1076C>G
|
ENSP00000404400.1:n.1076C>G
|
|
ENST00000434810.5:c.369C>G
|
|
|
ENST00000448511.5:c.1028C>G
|
ENSP00000404567.1:n.1028C>G
|
|
ENST00000456369.5:c.263+4007C>G
|
|
|
NM_001005735.1:c.1267C>G
|
NP_001005735.1:p.Leu423Val
|
|
NM_001257387.1:c.475C>G
|
NP_001244316.1:p.Leu159Val
|
|
NM_007194.3:c.1138C>G
|
NP_009125.1:p.Leu380Val
|
|
NM_145862.2:c.1051C>G
|
NP_665861.1:p.Leu351Val
|
|
XM_006724114.2:c.658C>G
|
XP_006724177.1:p.Leu220Val
|
|
XM_006724116.2:c.595C>G
|
XP_006724179.2:p.Leu199Val
|
|
XM_011529839.1:c.1297C>G
|
XP_011528141.1:p.Leu433Val
|
|
XM_011529840.1:c.1210C>G
|
XP_011528142.1:p.Leu404Val
|
|
XM_011529841.1:c.1066C>G
|
XP_011528143.1:p.Leu356Val
|
|
XM_011529842.1:c.967C>G
|
XP_011528144.1:p.Leu323Val
|
|
XM_011529843.1:c.937C>G
|
XP_011528145.1:p.Leu313Val
|
|
XM_011529845.1:c.475C>G
|
XP_011528147.1:p.Leu159Val
|
|
XR_937805.1:n.1297C>G
|
|
|
XR_937806.1:n.1205C>G
|
|
|
NM_001349956.1:c.937C>G
|
NP_001336885.1:p.Leu313Val
|
|
NM_007194.4:c.1138C>G
MANE Select
|
NP_009125.1:p.Leu380Val
|
|
XM_006724114.3:c.691C>G
|
XP_006724177.2:p.Leu231Val
|
|
XM_011529839.2:c.1297C>G
|
XP_011528141.1:p.Leu433Val
|
|
XM_011529840.3:c.1210C>G
|
XP_011528142.1:p.Leu404Val
|
|
XM_011529842.2:c.967C>G
|
XP_011528144.1:p.Leu323Val
|
|
XM_011529845.2:c.475C>G
|
XP_011528147.1:p.Leu159Val
|
|
XM_017028560.1:c.1261C>G
|
XP_016884049.1:p.Leu421Val
|
|
XM_017028561.2:c.475C>G
|
XP_016884050.1:p.Leu159Val
|
|
XM_024452148.1:c.1168C>G
|
XP_024307916.1:p.Leu390Val
|
|
XM_024452149.1:c.1081C>G
|
XP_024307917.1:p.Leu361Val
|
|
XR_937805.2:n.1308C>G
|
|
|
XR_937806.2:n.1221C>G
|
|
|
NM_001005735.2:c.1267C>G
|
NP_001005735.1:p.Leu423Val
|
|
NM_001257387.2:c.475C>G
|
NP_001244316.1:p.Leu159Val
|
|
NM_001349956.2:c.937C>G
|
NP_001336885.1:p.Leu313Val
|
|