ENST00000373327.5:c.1902G>C
MANE Select
|
ENSP00000362424.4:p.Gln634His
|
|
ENST00000373327.4:c.1902G>C
|
ENSP00000362424.4:p.Gln634His
|
|
ENST00000391993.7:c.1704G>C
|
ENSP00000375851.3:p.Gln568His
|
|
ENST00000462122.1:n.913G>C
|
|
|
ENST00000483951.1:n.250G>C
|
|
|
NM_001139490.1:c.1704G>C
|
NP_001132962.1:p.Gln568His
|
|
NM_015650.3:c.1902G>C
|
NP_056465.2:p.Gln634His
|
|
XM_006712414.1:c.1701G>C
|
XP_006712477.1:p.Gln567His
|
|
XM_011510944.1:c.2004G>C
|
XP_011509246.1:p.Gln668His
|
|
XM_011510945.1:c.1965G>C
|
XP_011509247.1:p.Gln655His
|
|
XM_011510946.1:c.1932G>C
|
XP_011509248.1:p.Gln644His
|
|
XM_011510947.1:c.1872G>C
|
XP_011509249.1:p.Gln624His
|
|
XM_011510948.1:c.1806G>C
|
XP_011509250.1:p.Gln602His
|
|
XM_011510950.1:c.870G>C
|
XP_011509252.1:p.Gln290His
|
|
XM_006712414.2:c.1701G>C
|
XP_006712477.1:p.Gln567His
|
|
XM_011510944.2:c.2004G>C
|
XP_011509246.1:p.Gln668His
|
|
XM_011510945.2:c.1965G>C
|
XP_011509247.1:p.Gln655His
|
|
XM_011510946.2:c.1932G>C
|
XP_011509248.1:p.Gln644His
|
|
XM_011510947.2:c.1872G>C
|
XP_011509249.1:p.Gln624His
|
|
XM_011510948.2:c.1806G>C
|
XP_011509250.1:p.Gln602His
|
|
XM_011510950.2:c.870G>C
|
XP_011509252.1:p.Gln290His
|
|
XM_017003789.1:c.2001G>C
|
XP_016859278.1:p.Gln667His
|
|
XR_001738696.1:n.1730G>C
|
|
|
XR_001738697.1:n.1727G>C
|
|
|
NM_015650.4:c.1902G>C
MANE Select
|
NP_056465.2:p.Gln634His
|
|