|
NM_000162.5:c.523G>C
MANE Select
|
NP_000153.1:p.Gly175Arg
|
|
ENST00000403799.8:c.523G>C
MANE Select
|
ENSP00000384247.3:p.Gly175Arg
|
|
NM_000162.3:c.523G>C
|
NP_000153.1:p.Gly175Arg
|
|
NM_000162.4:c.523G>C
|
NP_000153.1:p.Gly175Arg
|
|
NM_001354800.1:c.523G>C
|
NP_001341729.1:p.Gly175Arg
|
|
NM_033507.1:c.526G>C
|
NP_277042.1:p.Gly176Arg
|
|
NM_033507.2:c.526G>C
|
NP_277042.1:p.Gly176Arg
|
|
NM_033507.3:c.526G>C
|
NP_277042.1:p.Gly176Arg
|
|
NM_033508.1:c.520G>C
|
NP_277043.1:p.Gly174Arg
|
|
NM_033508.2:c.520G>C
|
NP_277043.1:p.Gly174Arg
|
|
NM_033508.3:c.520G>C
|
NP_277043.1:p.Gly174Arg
|
|
ENST00000345378.6:c.526G>C
|
ENSP00000223366.2:p.Gly176Arg
|
|
ENST00000345378.7:c.526G>C
|
ENSP00000223366.2:p.Gly176Arg
|
|
ENST00000395796.7:c.520G>C
|
ENSP00000379142.3:p.Gly174Arg
|
|
ENST00000395796.8:c.*521G>C
|
ENSP00000379142.4:n.*521G>C
|
|
ENST00000403799.7:c.523G>C
|
ENSP00000384247.3:p.Gly175Arg
|
|
ENST00000437084.1:c.472G>C
|
ENSP00000402840.1:p.Gly158Arg
|
|
ENST00000616242.4:c.520G>C
|
ENSP00000482149.1:p.Gly174Arg
|
|
ENST00000616242.5:c.523G>C
|
ENSP00000482149.2:p.Gly175Arg
|
|
ENST00000671824.1:c.523G>C
|
ENSP00000500264.1:p.Gly175Arg
|
|
ENST00000673284.1:c.523G>C
|
ENSP00000499852.1:p.Gly175Arg
|
|
ENST00000682635.1:n.1009G>C
|
|
