ENST00000302804.12:c.641G>T
MANE Select
|
ENSP00000302898.6:p.Arg214Ile
|
|
ENST00000302804.11:c.641G>T
|
ENSP00000302898.6:p.Arg214Ile
|
|
ENST00000415300.6:c.584G>T
|
ENSP00000407162.1:p.Arg195Ile
|
|
ENST00000448930.5:c.536G>T
|
ENSP00000406798.2:p.Arg179Ile
|
|
ENST00000594599.1:c.125G>T
|
ENSP00000469894.1:p.Arg42Ile
|
|
ENST00000596375.1:c.*202G>T
|
ENSP00000470465.1:n.*202G>T
|
|
ENST00000598785.5:c.539G>T
|
ENSP00000471830.1:p.Arg180Ile
|
|
ENST00000599062.5:c.632G>T
|
ENSP00000469983.1:p.Arg211Ile
|
|
ENST00000601799.5:c.*940G>T
|
ENSP00000468918.1:n.*940G>T
|
|
NM_001015878.1:c.641G>T
|
NP_001015878.1:p.Arg214Ile
|
|
NM_001015879.1:c.584G>T
|
NP_001015879.1:p.Arg195Ile
|
|
NM_003160.2:c.539G>T
|
NP_003151.2:p.Arg180Ile
|
|
XR_430209.2:n.1535G>T
|
|
|
XR_430209.3:n.1578G>T
|
|
|
NM_001015878.2:c.641G>T
MANE Select
|
NP_001015878.1:p.Arg214Ile
|
|
NM_001015879.2:c.584G>T
|
NP_001015879.1:p.Arg195Ile
|
|
NM_003160.3:c.539G>T
|
NP_003151.2:p.Arg180Ile
|
|