ENST00000373327.5:c.1845G>T
MANE Select
|
ENSP00000362424.4:p.Gln615His
|
|
ENST00000373327.4:c.1845G>T
|
ENSP00000362424.4:p.Gln615His
|
|
ENST00000391993.7:c.1647G>T
|
ENSP00000375851.3:p.Gln549His
|
|
ENST00000462122.1:n.856G>T
|
|
|
ENST00000483951.1:n.193G>T
|
|
|
NM_001139490.1:c.1647G>T
|
NP_001132962.1:p.Gln549His
|
|
NM_015650.3:c.1845G>T
|
NP_056465.2:p.Gln615His
|
|
XM_006712414.1:c.1644G>T
|
XP_006712477.1:p.Gln548His
|
|
XM_011510944.1:c.1947G>T
|
XP_011509246.1:p.Gln649His
|
|
XM_011510945.1:c.1908G>T
|
XP_011509247.1:p.Gln636His
|
|
XM_011510946.1:c.1875G>T
|
XP_011509248.1:p.Gln625His
|
|
XM_011510947.1:c.1815G>T
|
XP_011509249.1:p.Gln605His
|
|
XM_011510948.1:c.1749G>T
|
XP_011509250.1:p.Gln583His
|
|
XM_011510950.1:c.813G>T
|
XP_011509252.1:p.Gln271His
|
|
XM_006712414.2:c.1644G>T
|
XP_006712477.1:p.Gln548His
|
|
XM_011510944.2:c.1947G>T
|
XP_011509246.1:p.Gln649His
|
|
XM_011510945.2:c.1908G>T
|
XP_011509247.1:p.Gln636His
|
|
XM_011510946.2:c.1875G>T
|
XP_011509248.1:p.Gln625His
|
|
XM_011510947.2:c.1815G>T
|
XP_011509249.1:p.Gln605His
|
|
XM_011510948.2:c.1749G>T
|
XP_011509250.1:p.Gln583His
|
|
XM_011510950.2:c.813G>T
|
XP_011509252.1:p.Gln271His
|
|
XM_017003789.1:c.1944G>T
|
XP_016859278.1:p.Gln648His
|
|
XR_001738696.1:n.1673G>T
|
|
|
XR_001738697.1:n.1670G>T
|
|
|
NM_015650.4:c.1845G>T
MANE Select
|
NP_056465.2:p.Gln615His
|
|