|
ENST00000260947.9:c.2314T>G
MANE Select
|
ENSP00000260947.4:p.Leu772Val
|
|
|
ENST00000421162.2:c.961T>G
|
ENSP00000392245.2:p.Leu321Val
|
|
|
ENST00000613192.2:c.*377T>G
|
ENSP00000483275.2:n.*377T>G
|
|
|
ENST00000613374.5:c.904T>G
|
ENSP00000484464.1:p.Leu302Val
|
|
|
ENST00000613706.5:c.1906T>G
|
ENSP00000484976.2:p.Leu636Val
|
|
|
ENST00000617164.5:c.2257T>G
|
ENSP00000480470.1:p.Leu753Val
|
|
|
ENST00000619009.5:c.775T>G
|
ENSP00000482293.1:p.Leu259Val
|
|
|
ENST00000650978.1:c.3689T>G
|
|
|
|
ENST00000260947.8:c.2314T>G
|
ENSP00000260947.4:p.Leu772Val
|
|
|
ENST00000432456.5:c.457T>G
|
|
|
|
ENST00000471590.5:n.649T>G
|
|
|
|
ENST00000613192.1:c.484T>G
|
ENSP00000483275.1:p.Leu162Val
|
|
|
ENST00000613374.4:c.904T>G
|
ENSP00000484464.1:p.Leu302Val
|
|
|
ENST00000613706.4:c.961T>G
|
ENSP00000484976.1:p.Leu321Val
|
|
|
ENST00000617164.4:c.2257T>G
|
ENSP00000480470.1:p.Leu753Val
|
|
|
ENST00000619009.4:c.775T>G
|
ENSP00000482293.1:p.Leu259Val
|
|
|
ENST00000620057.4:c.*980T>G
|
ENSP00000481988.1:n.*980T>G
|
|
|
NM_000465.3:c.2314T>G
|
NP_000456.2:p.Leu772Val
|
|
|
NM_001282543.1:c.2257T>G
|
NP_001269472.1:p.Leu753Val
|
|
|
NM_001282545.1:c.961T>G
|
NP_001269474.1:p.Leu321Val
|
|
|
NM_001282548.1:c.904T>G
|
NP_001269477.1:p.Leu302Val
|
|
|
NM_001282549.1:c.775T>G
|
NP_001269478.1:p.Leu259Val
|
|
|
NR_104212.1:n.2307T>G
|
|
|
|
NR_104215.1:n.2250T>G
|
|
|
|
NR_104216.1:n.1506T>G
|
|
|
|
XM_011511567.1:c.2260T>G
|
XP_011509869.1:p.Leu754Val
|
|
|
XM_017004613.1:c.2413T>G
|
XP_016860102.1:p.Leu805Val
|
|
|
XR_002959322.1:n.2680T>G
|
|
|
|
NM_000465.4:c.2314T>G
MANE Select
|
NP_000456.2:p.Leu772Val
|
|
|
NM_001282543.2:c.2257T>G
|
NP_001269472.1:p.Leu753Val
|
|
|
NM_001282545.2:c.961T>G
|
NP_001269474.1:p.Leu321Val
|
|
|
NM_001282548.2:c.904T>G
|
NP_001269477.1:p.Leu302Val
|
|
|
NM_001282549.2:c.775T>G
|
NP_001269478.1:p.Leu259Val
|
|
|
NR_104212.2:n.2279T>G
|
|
|
|
NR_104215.2:n.2222T>G
|
|
|
|
NR_104216.2:n.1478T>G
|
|
|
