ENST00000324444.9:c.852G>C
MANE Select
|
ENSP00000316130.3:p.Arg284Ser
|
|
ENST00000397428.8:c.67-1001G>C
|
|
|
ENST00000465425.2:n.964G>C
|
|
|
ENST00000324444.7:c.852G>C
|
ENSP00000316130.3:p.Arg284Ser
|
|
ENST00000340477.9:c.513G>C
|
ENSP00000343152.5:p.Arg171Ser
|
|
ENST00000397428.7:c.40-1001G>C
|
ENSP00000380572.3:n.40-1001G>C
|
|
ENST00000465425.1:n.964G>C
|
|
|
ENST00000490730.1:c.688+164G>C
|
ENSP00000422716.1:n.688+164G>C
|
|
ENST00000503121.5:c.242+1779G>C
|
|
|
ENST00000505054.2:n.395-1001G>C
|
|
|
NM_001039876.1:c.852G>C
|
NP_001034965.1:p.Arg284Ser
|
|
NM_001039876.2:c.852G>C
|
NP_001034965.1:p.Arg284Ser
|
|
NM_001297735.1:c.513G>C
|
NP_001284664.1:p.Arg171Ser
|
|
NM_001297735.2:c.513G>C
|
NP_001284664.1:p.Arg171Ser
|
|
XM_005258598.2:c.688+164G>C
|
XP_005258655.1:n.688+164G>C
|
|
XM_005258601.2:c.618+312G>C
|
XP_005258658.1:n.618+312G>C
|
|
XM_005258604.3:c.688+164G>C
|
XP_005258661.1:n.688+164G>C
|
|
NM_001039876.3:c.852G>C
MANE Select
|
NP_001034965.1:p.Arg284Ser
|
|
NM_001297735.3:c.513G>C
|
NP_001284664.1:p.Arg171Ser
|
|