ENST00000260947.9:c.1892T>A
MANE Select
|
ENSP00000260947.4:p.Leu631Gln
|
|
ENST00000421162.2:c.539T>A
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ENSP00000392245.2:p.Leu180Gln
|
|
ENST00000613192.2:c.159-14570T>A
|
ENSP00000483275.2:n.159-14570T>A
|
|
ENST00000613374.5:c.482T>A
|
ENSP00000484464.1:p.Leu161Gln
|
|
ENST00000613706.5:c.1484T>A
|
ENSP00000484976.2:p.Leu495Gln
|
|
ENST00000617164.5:c.1835T>A
|
ENSP00000480470.1:p.Leu612Gln
|
|
ENST00000619009.5:c.365-14570T>A
|
ENSP00000482293.1:n.365-14570T>A
|
|
ENST00000650978.1:c.3267T>A
|
|
|
ENST00000260947.8:c.1892T>A
|
ENSP00000260947.4:p.Leu631Gln
|
|
ENST00000421162.1:c.539T>A
|
ENSP00000392245.1:p.Leu180Gln
|
|
ENST00000455743.5:c.*1512T>A
|
ENSP00000412186.1:n.*1512T>A
|
|
ENST00000613192.1:c.74-14570T>A
|
ENSP00000483275.1:n.74-14570T>A
|
|
ENST00000613374.4:c.482T>A
|
ENSP00000484464.1:p.Leu161Gln
|
|
ENST00000613706.4:c.539T>A
|
ENSP00000484976.1:p.Leu180Gln
|
|
ENST00000617164.4:c.1835T>A
|
ENSP00000480470.1:p.Leu612Gln
|
|
ENST00000619009.4:c.365-14570T>A
|
ENSP00000482293.1:n.365-14570T>A
|
|
ENST00000620057.4:c.*558T>A
|
ENSP00000481988.1:n.*558T>A
|
|
NM_000465.3:c.1892T>A
|
NP_000456.2:p.Leu631Gln
|
|
NM_001282543.1:c.1835T>A
|
NP_001269472.1:p.Leu612Gln
|
|
NM_001282545.1:c.539T>A
|
NP_001269474.1:p.Leu180Gln
|
|
NM_001282548.1:c.482T>A
|
NP_001269477.1:p.Leu161Gln
|
|
NM_001282549.1:c.365-14570T>A
|
NP_001269478.1:n.365-14570T>A
|
|
NR_104212.1:n.1885T>A
|
|
|
NR_104215.1:n.1828T>A
|
|
|
NR_104216.1:n.1084T>A
|
|
|
XM_011511567.1:c.1838T>A
|
XP_011509869.1:p.Leu613Gln
|
|
XM_011511568.1:c.1892T>A
|
XP_011509870.1:p.Leu631Gln
|
|
XM_017004613.1:c.1991T>A
|
XP_016860102.1:p.Leu664Gln
|
|
XM_017004614.1:c.1991T>A
|
XP_016860103.1:p.Leu664Gln
|
|
XR_002959322.1:n.2082T>A
|
|
|
NM_000465.4:c.1892T>A
MANE Select
|
NP_000456.2:p.Leu631Gln
|
|
NM_001282543.2:c.1835T>A
|
NP_001269472.1:p.Leu612Gln
|
|
NM_001282545.2:c.539T>A
|
NP_001269474.1:p.Leu180Gln
|
|
NM_001282548.2:c.482T>A
|
NP_001269477.1:p.Leu161Gln
|
|
NM_001282549.2:c.365-14570T>A
|
NP_001269478.1:n.365-14570T>A
|
|
NR_104212.2:n.1857T>A
|
|
|
NR_104215.2:n.1800T>A
|
|
|
NR_104216.2:n.1056T>A
|
|
|