|
ENST00000703936.1:c.2693T>G
|
ENSP00000515567.1:p.Leu898Arg
|
|
|
ENST00000703937.1:c.*1754T>G
|
ENSP00000515568.1:n.*1754T>G
|
|
|
ENST00000326739.9:c.653T>G
MANE Select
|
ENSP00000321584.4:p.Leu218Arg
|
|
|
ENST00000429182.6:c.653T>G
|
ENSP00000393525.2:p.Leu218Arg
|
|
|
ENST00000442157.2:c.578T>G
|
ENSP00000403502.2:p.Leu193Arg
|
|
|
ENST00000462980.2:n.1168T>G
|
|
|
|
ENST00000472328.2:n.719T>G
|
|
|
|
ENST00000491610.2:n.613T>G
|
|
|
|
ENST00000676607.1:n.949T>G
|
|
|
|
ENST00000676627.1:n.1383T>G
|
|
|
|
ENST00000676708.1:n.1933T>G
|
|
|
|
ENST00000676864.1:n.1802T>G
|
|
|
|
ENST00000677010.1:c.689T>G
|
ENSP00000503089.1:p.Leu230Arg
|
|
|
ENST00000677108.1:n.2559T>G
|
|
|
|
ENST00000677168.1:n.1125T>G
|
|
|
|
ENST00000677185.1:n.1216T>G
|
|
|
|
ENST00000677205.1:n.1437T>G
|
|
|
|
ENST00000677344.1:n.1927T>G
|
|
|
|
ENST00000677480.1:c.*330T>G
|
ENSP00000504378.1:n.*330T>G
|
|
|
ENST00000677519.1:n.1363T>G
|
|
|
|
ENST00000677593.1:n.1209T>G
|
|
|
|
ENST00000677740.1:n.2158T>G
|
|
|
|
ENST00000677991.1:n.1826T>G
|
|
|
|
ENST00000678001.1:n.1146T>G
|
|
|
|
ENST00000678085.1:n.1209T>G
|
|
|
|
ENST00000678177.1:n.2502T>G
|
|
|
|
ENST00000678603.1:n.1731T>G
|
|
|
|
ENST00000678724.1:c.578T>G
|
ENSP00000503874.1:p.Leu193Arg
|
|
|
ENST00000678920.1:n.811T>G
|
|
|
|
ENST00000679019.1:n.1423T>G
|
|
|
|
ENST00000679117.1:c.*468T>G
|
ENSP00000503240.1:n.*468T>G
|
|
|
ENST00000679339.1:n.1494T>G
|
|
|
|
ENST00000326739.8:c.653T>G
|
ENSP00000321584.4:p.Leu218Arg
|
|
|
ENST00000429182.5:c.447T>G
|
|
|
|
ENST00000442157.1:c.578T>G
|
ENSP00000403502.1:p.Leu193Arg
|
|
|
ENST00000462980.1:n.555T>G
|
|
|
|
ENST00000491610.1:n.613T>G
|
|
|
|
NM_000884.2:c.653T>G
|
NP_000875.2:p.Leu218Arg
|
|
|
XM_006713128.2:c.863T>G
|
XP_006713191.1:p.Leu288Arg
|
|
|
XM_006713128.3:c.863T>G
|
XP_006713191.1:p.Leu288Arg
|
|
|
XM_017006349.1:c.788T>G
|
XP_016861838.1:p.Leu263Arg
|
|
|
XM_017006350.1:c.788T>G
|
XP_016861839.1:p.Leu263Arg
|
|
|
NM_000884.3:c.653T>G
MANE Select
|
NP_000875.2:p.Leu218Arg
|
|
