ENST00000373327.5:c.1888G>C
MANE Select
|
ENSP00000362424.4:p.Glu630Gln
|
|
ENST00000373327.4:c.1888G>C
|
ENSP00000362424.4:p.Glu630Gln
|
|
ENST00000391993.7:c.1690G>C
|
ENSP00000375851.3:p.Glu564Gln
|
|
ENST00000462122.1:n.899G>C
|
|
|
ENST00000483951.1:n.236G>C
|
|
|
NM_001139490.1:c.1690G>C
|
NP_001132962.1:p.Glu564Gln
|
|
NM_015650.3:c.1888G>C
|
NP_056465.2:p.Glu630Gln
|
|
XM_006712414.1:c.1687G>C
|
XP_006712477.1:p.Glu563Gln
|
|
XM_011510944.1:c.1990G>C
|
XP_011509246.1:p.Glu664Gln
|
|
XM_011510945.1:c.1951G>C
|
XP_011509247.1:p.Glu651Gln
|
|
XM_011510946.1:c.1918G>C
|
XP_011509248.1:p.Glu640Gln
|
|
XM_011510947.1:c.1858G>C
|
XP_011509249.1:p.Glu620Gln
|
|
XM_011510948.1:c.1792G>C
|
XP_011509250.1:p.Glu598Gln
|
|
XM_011510950.1:c.856G>C
|
XP_011509252.1:p.Glu286Gln
|
|
XM_006712414.2:c.1687G>C
|
XP_006712477.1:p.Glu563Gln
|
|
XM_011510944.2:c.1990G>C
|
XP_011509246.1:p.Glu664Gln
|
|
XM_011510945.2:c.1951G>C
|
XP_011509247.1:p.Glu651Gln
|
|
XM_011510946.2:c.1918G>C
|
XP_011509248.1:p.Glu640Gln
|
|
XM_011510947.2:c.1858G>C
|
XP_011509249.1:p.Glu620Gln
|
|
XM_011510948.2:c.1792G>C
|
XP_011509250.1:p.Glu598Gln
|
|
XM_011510950.2:c.856G>C
|
XP_011509252.1:p.Glu286Gln
|
|
XM_017003789.1:c.1987G>C
|
XP_016859278.1:p.Glu663Gln
|
|
XR_001738696.1:n.1716G>C
|
|
|
XR_001738697.1:n.1713G>C
|
|
|
NM_015650.4:c.1888G>C
MANE Select
|
NP_056465.2:p.Glu630Gln
|
|