ENST00000703936.1:c.2743C>G
|
ENSP00000515567.1:p.Leu915Val
|
|
ENST00000703937.1:c.*1804C>G
|
ENSP00000515568.1:n.*1804C>G
|
|
ENST00000326739.9:c.703C>G
MANE Select
|
ENSP00000321584.4:p.Leu235Val
|
|
ENST00000429182.6:c.703C>G
|
ENSP00000393525.2:p.Leu235Val
|
|
ENST00000442157.2:c.628C>G
|
ENSP00000403502.2:p.Leu210Val
|
|
ENST00000462980.2:n.1218C>G
|
|
|
ENST00000472328.2:n.769C>G
|
|
|
ENST00000491610.2:n.663C>G
|
|
|
ENST00000676607.1:n.999C>G
|
|
|
ENST00000676627.1:n.1433C>G
|
|
|
ENST00000676708.1:n.1983C>G
|
|
|
ENST00000676864.1:n.1852C>G
|
|
|
ENST00000677010.1:c.739C>G
|
ENSP00000503089.1:p.Leu247Val
|
|
ENST00000677108.1:n.2609C>G
|
|
|
ENST00000677168.1:n.1175C>G
|
|
|
ENST00000677185.1:n.1266C>G
|
|
|
ENST00000677205.1:n.1487C>G
|
|
|
ENST00000677344.1:n.1977C>G
|
|
|
ENST00000677480.1:c.*380C>G
|
ENSP00000504378.1:n.*380C>G
|
|
ENST00000677519.1:n.1413C>G
|
|
|
ENST00000677593.1:n.1259C>G
|
|
|
ENST00000677740.1:n.2208C>G
|
|
|
ENST00000677991.1:n.1876C>G
|
|
|
ENST00000678001.1:n.1196C>G
|
|
|
ENST00000678085.1:n.1259C>G
|
|
|
ENST00000678177.1:n.2552C>G
|
|
|
ENST00000678603.1:n.1781C>G
|
|
|
ENST00000678724.1:c.628C>G
|
ENSP00000503874.1:p.Leu210Val
|
|
ENST00000678920.1:n.861C>G
|
|
|
ENST00000679019.1:n.1473C>G
|
|
|
ENST00000679117.1:c.*518C>G
|
ENSP00000503240.1:n.*518C>G
|
|
ENST00000679339.1:n.1544C>G
|
|
|
ENST00000326739.8:c.703C>G
|
ENSP00000321584.4:p.Leu235Val
|
|
ENST00000429182.5:c.497C>G
|
|
|
ENST00000442157.1:c.628C>G
|
ENSP00000403502.1:p.Leu210Val
|
|
ENST00000462980.1:n.605C>G
|
|
|
ENST00000491610.1:n.663C>G
|
|
|
NM_000884.2:c.703C>G
|
NP_000875.2:p.Leu235Val
|
|
XM_006713128.2:c.913C>G
|
XP_006713191.1:p.Leu305Val
|
|
XM_006713128.3:c.913C>G
|
XP_006713191.1:p.Leu305Val
|
|
XM_017006349.1:c.838C>G
|
XP_016861838.1:p.Leu280Val
|
|
XM_017006350.1:c.838C>G
|
XP_016861839.1:p.Leu280Val
|
|
NM_000884.3:c.703C>G
MANE Select
|
NP_000875.2:p.Leu235Val
|
|