ENST00000446859.7:c.870G>A
MANE Select
|
ENSP00000414635.1:p.Leu290=
|
|
ENST00000446859.5:c.870G>A
|
ENSP00000414635.1:p.Leu290=
|
|
ENST00000522080.5:n.847G>A
|
|
|
ENST00000522329.1:n.119G>A
|
|
|
ENST00000522526.6:c.774G>A
|
ENSP00000429278.2:p.Leu258=
|
|
ENST00000522596.6:n.852G>A
|
|
|
ENST00000522830.5:c.687G>A
|
ENSP00000429593.1:p.Leu229=
|
|
ENST00000524054.5:n.718G>A
|
|
|
ENST00000524327.5:n.670G>A
|
|
|
ENST00000528597.1:c.117G>A
|
ENSP00000436883.1:p.Leu39=
|
|
ENST00000602774.1:n.256G>A
|
|
|
NM_001172779.1:c.870G>A
|
NP_001166250.1:p.Leu290=
|
|
NM_001172780.1:c.870G>A
|
NP_001166251.1:p.Leu290=
|
|
NM_153353.4:c.774G>A
|
NP_699184.2:p.Leu258=
|
|
XM_005247133.2:c.687G>A
|
XP_005247190.1:p.Leu229=
|
|
XM_006713508.2:c.816G>A
|
XP_006713571.1:p.Leu272=
|
|
XM_011512442.1:c.867G>A
|
XP_011510744.1:p.Leu289=
|
|
NM_001363888.1:c.687G>A
|
NP_001350817.1:p.Leu229=
|
|
XM_006713508.4:c.816G>A
|
XP_006713571.1:p.Leu272=
|
|
XM_011512442.2:c.867G>A
|
XP_011510744.1:p.Leu289=
|
|
XM_017005746.1:c.684G>A
|
XP_016861235.1:p.Leu228=
|
|
NM_001172779.2:c.870G>A
MANE Select
|
NP_001166250.1:p.Leu290=
|
|
NM_001172780.2:c.870G>A
|
NP_001166251.1:p.Leu290=
|
|
NM_001363888.2:c.687G>A
|
NP_001350817.1:p.Leu229=
|
|
NM_001370608.1:c.684G>A
|
NP_001357537.1:p.Leu228=
|
|
NM_001370609.1:c.687G>A
|
NP_001357538.1:p.Leu229=
|
|
NM_153353.5:c.774G>A
|
NP_699184.2:p.Leu258=
|
|