|
ENST00000382099.3:c.1005C>G
|
|
|
|
ENST00000382100.8:c.1447C>G
MANE Select
|
ENSP00000371532.2:p.Leu483Val
|
|
|
ENST00000478776.2:n.892C>G
|
|
|
|
ENST00000679718.1:n.683C>G
|
|
|
|
ENST00000679750.1:n.863C>G
|
|
|
|
ENST00000679851.1:n.1631C>G
|
|
|
|
ENST00000680021.1:n.1647C>G
|
|
|
|
ENST00000680043.1:c.999C>G
|
|
|
|
ENST00000680219.1:c.1014C>G
|
|
|
|
ENST00000680243.1:c.*1226C>G
|
ENSP00000505911.1:n.*1226C>G
|
|
|
ENST00000680296.1:c.873C>G
|
|
|
|
ENST00000680332.1:n.530C>G
|
|
|
|
ENST00000680746.1:c.1324C>G
|
ENSP00000505030.1:p.Leu442Val
|
|
|
ENST00000680751.1:n.852C>G
|
|
|
|
ENST00000680891.1:c.*1239C>G
|
ENSP00000505167.1:n.*1239C>G
|
|
|
ENST00000680975.1:n.832C>G
|
|
|
|
ENST00000681087.1:n.892C>G
|
|
|
|
ENST00000681306.1:c.1447C>G
|
ENSP00000506072.1:p.Leu483Val
|
|
|
ENST00000681618.1:c.1324C>G
|
ENSP00000505773.1:p.Leu442Val
|
|
|
ENST00000681644.1:c.*1119C>G
|
ENSP00000505180.1:n.*1119C>G
|
|
|
ENST00000681806.1:c.1447C>G
|
ENSP00000505282.1:p.Leu483Val
|
|
|
ENST00000681942.1:c.995C>G
|
|
|
|
ENST00000382099.2:c.1447C>G
|
ENSP00000371531.2:p.Leu483Val
|
|
|
ENST00000382100.7:c.1447C>G
|
ENSP00000371532.2:p.Leu483Val
|
|
|
NM_001018056.1:c.1447C>G
|
NP_001018066.1:p.Leu483Val
|
|
|
NM_003383.3:c.1447C>G
|
NP_003374.3:p.Leu483Val
|
|
|
XM_011518029.1:c.1324C>G
|
XP_011516331.1:p.Leu442Val
|
|
|
NM_001018056.2:c.1447C>G
|
NP_001018066.1:p.Leu483Val
|
|
|
NM_001322225.1:c.1324C>G
|
NP_001309154.1:p.Leu442Val
|
|
|
NM_001322226.1:c.1324C>G
|
NP_001309155.1:p.Leu442Val
|
|
|
NM_003383.4:c.1447C>G
|
NP_003374.3:p.Leu483Val
|
|
|
XR_001746373.2:n.1851C>G
|
|
|
|
XR_002956805.1:n.1851C>G
|
|
|
|
NM_003383.5:c.1447C>G
MANE Select
|
NP_003374.3:p.Leu483Val
|
|
|
NM_001018056.3:c.1447C>G
|
NP_001018066.1:p.Leu483Val
|
|
|
NM_001322225.2:c.1324C>G
|
NP_001309154.1:p.Leu442Val
|
|
|
NM_001322226.2:c.1324C>G
|
NP_001309155.1:p.Leu442Val
|
|
