|
ENST00000703936.1:c.2827C>G
|
ENSP00000515567.1:p.Leu943Val
|
|
|
ENST00000703937.1:c.*1888C>G
|
ENSP00000515568.1:n.*1888C>G
|
|
|
ENST00000326739.9:c.787C>G
MANE Select
|
ENSP00000321584.4:p.Leu263Val
|
|
|
ENST00000429182.6:c.787C>G
|
ENSP00000393525.2:p.Leu263Val
|
|
|
ENST00000442157.2:c.712C>G
|
ENSP00000403502.2:p.Leu238Val
|
|
|
ENST00000462980.2:n.1302C>G
|
|
|
|
ENST00000472328.2:n.853C>G
|
|
|
|
ENST00000491610.2:n.747C>G
|
|
|
|
ENST00000676607.1:n.1083C>G
|
|
|
|
ENST00000676627.1:n.1517C>G
|
|
|
|
ENST00000676708.1:n.2067C>G
|
|
|
|
ENST00000676864.1:n.1936C>G
|
|
|
|
ENST00000677010.1:c.823C>G
|
ENSP00000503089.1:p.Leu275Val
|
|
|
ENST00000677108.1:n.2693C>G
|
|
|
|
ENST00000677168.1:n.1259C>G
|
|
|
|
ENST00000677185.1:n.1350C>G
|
|
|
|
ENST00000677205.1:n.1571C>G
|
|
|
|
ENST00000677344.1:n.2061C>G
|
|
|
|
ENST00000677480.1:c.*464C>G
|
ENSP00000504378.1:n.*464C>G
|
|
|
ENST00000677519.1:n.1497C>G
|
|
|
|
ENST00000677593.1:n.1343C>G
|
|
|
|
ENST00000677740.1:n.2292C>G
|
|
|
|
ENST00000677991.1:n.1960C>G
|
|
|
|
ENST00000678001.1:n.1280C>G
|
|
|
|
ENST00000678085.1:n.1343C>G
|
|
|
|
ENST00000678177.1:n.2636C>G
|
|
|
|
ENST00000678603.1:n.1865C>G
|
|
|
|
ENST00000678724.1:c.712C>G
|
ENSP00000503874.1:p.Leu238Val
|
|
|
ENST00000678920.1:n.945C>G
|
|
|
|
ENST00000679019.1:n.1557C>G
|
|
|
|
ENST00000679117.1:c.*602C>G
|
ENSP00000503240.1:n.*602C>G
|
|
|
ENST00000679339.1:n.1628C>G
|
|
|
|
ENST00000326739.8:c.787C>G
|
ENSP00000321584.4:p.Leu263Val
|
|
|
ENST00000429182.5:c.581C>G
|
|
|
|
ENST00000442157.1:c.712C>G
|
ENSP00000403502.1:p.Leu238Val
|
|
|
ENST00000462980.1:n.689C>G
|
|
|
|
ENST00000491610.1:n.747C>G
|
|
|
|
NM_000884.2:c.787C>G
|
NP_000875.2:p.Leu263Val
|
|
|
XM_006713128.2:c.997C>G
|
XP_006713191.1:p.Leu333Val
|
|
|
XM_006713128.3:c.997C>G
|
XP_006713191.1:p.Leu333Val
|
|
|
XM_017006349.1:c.922C>G
|
XP_016861838.1:p.Leu308Val
|
|
|
XM_017006350.1:c.922C>G
|
XP_016861839.1:p.Leu308Val
|
|
|
NM_000884.3:c.787C>G
MANE Select
|
NP_000875.2:p.Leu263Val
|
|
