ENST00000373327.5:c.1857G>C
MANE Select
|
ENSP00000362424.4:p.Gln619His
|
|
ENST00000373327.4:c.1857G>C
|
ENSP00000362424.4:p.Gln619His
|
|
ENST00000391993.7:c.1659G>C
|
ENSP00000375851.3:p.Gln553His
|
|
ENST00000462122.1:n.868G>C
|
|
|
ENST00000483951.1:n.205G>C
|
|
|
NM_001139490.1:c.1659G>C
|
NP_001132962.1:p.Gln553His
|
|
NM_015650.3:c.1857G>C
|
NP_056465.2:p.Gln619His
|
|
XM_006712414.1:c.1656G>C
|
XP_006712477.1:p.Gln552His
|
|
XM_011510944.1:c.1959G>C
|
XP_011509246.1:p.Gln653His
|
|
XM_011510945.1:c.1920G>C
|
XP_011509247.1:p.Gln640His
|
|
XM_011510946.1:c.1887G>C
|
XP_011509248.1:p.Gln629His
|
|
XM_011510947.1:c.1827G>C
|
XP_011509249.1:p.Gln609His
|
|
XM_011510948.1:c.1761G>C
|
XP_011509250.1:p.Gln587His
|
|
XM_011510950.1:c.825G>C
|
XP_011509252.1:p.Gln275His
|
|
XM_006712414.2:c.1656G>C
|
XP_006712477.1:p.Gln552His
|
|
XM_011510944.2:c.1959G>C
|
XP_011509246.1:p.Gln653His
|
|
XM_011510945.2:c.1920G>C
|
XP_011509247.1:p.Gln640His
|
|
XM_011510946.2:c.1887G>C
|
XP_011509248.1:p.Gln629His
|
|
XM_011510947.2:c.1827G>C
|
XP_011509249.1:p.Gln609His
|
|
XM_011510948.2:c.1761G>C
|
XP_011509250.1:p.Gln587His
|
|
XM_011510950.2:c.825G>C
|
XP_011509252.1:p.Gln275His
|
|
XM_017003789.1:c.1956G>C
|
XP_016859278.1:p.Gln652His
|
|
XR_001738696.1:n.1685G>C
|
|
|
XR_001738697.1:n.1682G>C
|
|
|
NM_015650.4:c.1857G>C
MANE Select
|
NP_056465.2:p.Gln619His
|
|