ENST00000373327.5:c.1854G>T
MANE Select
|
ENSP00000362424.4:p.Leu618=
|
|
ENST00000373327.4:c.1854G>T
|
ENSP00000362424.4:p.Leu618=
|
|
ENST00000391993.7:c.1656G>T
|
ENSP00000375851.3:p.Leu552=
|
|
ENST00000462122.1:n.865G>T
|
|
|
ENST00000483951.1:n.202G>T
|
|
|
NM_001139490.1:c.1656G>T
|
NP_001132962.1:p.Leu552=
|
|
NM_015650.3:c.1854G>T
|
NP_056465.2:p.Leu618=
|
|
XM_006712414.1:c.1653G>T
|
XP_006712477.1:p.Leu551=
|
|
XM_011510944.1:c.1956G>T
|
XP_011509246.1:p.Leu652=
|
|
XM_011510945.1:c.1917G>T
|
XP_011509247.1:p.Leu639=
|
|
XM_011510946.1:c.1884G>T
|
XP_011509248.1:p.Leu628=
|
|
XM_011510947.1:c.1824G>T
|
XP_011509249.1:p.Leu608=
|
|
XM_011510948.1:c.1758G>T
|
XP_011509250.1:p.Leu586=
|
|
XM_011510950.1:c.822G>T
|
XP_011509252.1:p.Leu274=
|
|
XM_006712414.2:c.1653G>T
|
XP_006712477.1:p.Leu551=
|
|
XM_011510944.2:c.1956G>T
|
XP_011509246.1:p.Leu652=
|
|
XM_011510945.2:c.1917G>T
|
XP_011509247.1:p.Leu639=
|
|
XM_011510946.2:c.1884G>T
|
XP_011509248.1:p.Leu628=
|
|
XM_011510947.2:c.1824G>T
|
XP_011509249.1:p.Leu608=
|
|
XM_011510948.2:c.1758G>T
|
XP_011509250.1:p.Leu586=
|
|
XM_011510950.2:c.822G>T
|
XP_011509252.1:p.Leu274=
|
|
XM_017003789.1:c.1953G>T
|
XP_016859278.1:p.Leu651=
|
|
XR_001738696.1:n.1682G>T
|
|
|
XR_001738697.1:n.1679G>T
|
|
|
NM_015650.4:c.1854G>T
MANE Select
|
NP_056465.2:p.Leu618=
|
|