ENST00000382099.3:c.950A>T
|
|
|
ENST00000382100.8:c.1392A>T
MANE Select
|
ENSP00000371532.2:p.Leu464=
|
|
ENST00000478776.2:n.837A>T
|
|
|
ENST00000679718.1:n.628A>T
|
|
|
ENST00000679750.1:n.808A>T
|
|
|
ENST00000679851.1:n.1576A>T
|
|
|
ENST00000680021.1:n.1592A>T
|
|
|
ENST00000680043.1:c.944A>T
|
|
|
ENST00000680219.1:c.959A>T
|
|
|
ENST00000680243.1:c.*1171A>T
|
ENSP00000505911.1:n.*1171A>T
|
|
ENST00000680296.1:c.818A>T
|
|
|
ENST00000680332.1:n.475A>T
|
|
|
ENST00000680746.1:c.1269A>T
|
ENSP00000505030.1:p.Leu423=
|
|
ENST00000680751.1:n.797A>T
|
|
|
ENST00000680891.1:c.*1184A>T
|
ENSP00000505167.1:n.*1184A>T
|
|
ENST00000680975.1:n.777A>T
|
|
|
ENST00000681087.1:n.837A>T
|
|
|
ENST00000681306.1:c.1392A>T
|
ENSP00000506072.1:p.Leu464=
|
|
ENST00000681618.1:c.1269A>T
|
ENSP00000505773.1:p.Leu423=
|
|
ENST00000681644.1:c.*1064A>T
|
ENSP00000505180.1:n.*1064A>T
|
|
ENST00000681806.1:c.1392A>T
|
ENSP00000505282.1:p.Leu464=
|
|
ENST00000681942.1:c.940A>T
|
|
|
ENST00000382099.2:c.1392A>T
|
ENSP00000371531.2:p.Leu464=
|
|
ENST00000382100.7:c.1392A>T
|
ENSP00000371532.2:p.Leu464=
|
|
NM_001018056.1:c.1392A>T
|
NP_001018066.1:p.Leu464=
|
|
NM_003383.3:c.1392A>T
|
NP_003374.3:p.Leu464=
|
|
XM_011518029.1:c.1269A>T
|
XP_011516331.1:p.Leu423=
|
|
NM_001018056.2:c.1392A>T
|
NP_001018066.1:p.Leu464=
|
|
NM_001322225.1:c.1269A>T
|
NP_001309154.1:p.Leu423=
|
|
NM_001322226.1:c.1269A>T
|
NP_001309155.1:p.Leu423=
|
|
NM_003383.4:c.1392A>T
|
NP_003374.3:p.Leu464=
|
|
XR_001746373.2:n.1796A>T
|
|
|
XR_002956805.1:n.1796A>T
|
|
|
NM_003383.5:c.1392A>T
MANE Select
|
NP_003374.3:p.Leu464=
|
|
NM_001018056.3:c.1392A>T
|
NP_001018066.1:p.Leu464=
|
|
NM_001322225.2:c.1269A>T
|
NP_001309154.1:p.Leu423=
|
|
NM_001322226.2:c.1269A>T
|
NP_001309155.1:p.Leu423=
|
|