ENST00000373327.5:c.1801G>C
MANE Select
|
ENSP00000362424.4:p.Gly601Arg
|
|
ENST00000373327.4:c.1801G>C
|
ENSP00000362424.4:p.Gly601Arg
|
|
ENST00000391993.7:c.1603G>C
|
ENSP00000375851.3:p.Gly535Arg
|
|
ENST00000462122.1:n.812G>C
|
|
|
ENST00000483951.1:n.149G>C
|
|
|
NM_001139490.1:c.1603G>C
|
NP_001132962.1:p.Gly535Arg
|
|
NM_015650.3:c.1801G>C
|
NP_056465.2:p.Gly601Arg
|
|
XM_006712414.1:c.1600G>C
|
XP_006712477.1:p.Gly534Arg
|
|
XM_011510944.1:c.1903G>C
|
XP_011509246.1:p.Gly635Arg
|
|
XM_011510945.1:c.1864G>C
|
XP_011509247.1:p.Gly622Arg
|
|
XM_011510946.1:c.1831G>C
|
XP_011509248.1:p.Gly611Arg
|
|
XM_011510947.1:c.1771G>C
|
XP_011509249.1:p.Gly591Arg
|
|
XM_011510948.1:c.1705G>C
|
XP_011509250.1:p.Gly569Arg
|
|
XM_011510950.1:c.769G>C
|
XP_011509252.1:p.Gly257Arg
|
|
XM_006712414.2:c.1600G>C
|
XP_006712477.1:p.Gly534Arg
|
|
XM_011510944.2:c.1903G>C
|
XP_011509246.1:p.Gly635Arg
|
|
XM_011510945.2:c.1864G>C
|
XP_011509247.1:p.Gly622Arg
|
|
XM_011510946.2:c.1831G>C
|
XP_011509248.1:p.Gly611Arg
|
|
XM_011510947.2:c.1771G>C
|
XP_011509249.1:p.Gly591Arg
|
|
XM_011510948.2:c.1705G>C
|
XP_011509250.1:p.Gly569Arg
|
|
XM_011510950.2:c.769G>C
|
XP_011509252.1:p.Gly257Arg
|
|
XM_017003789.1:c.1900G>C
|
XP_016859278.1:p.Gly634Arg
|
|
XR_001738696.1:n.1629G>C
|
|
|
XR_001738697.1:n.1626G>C
|
|
|
NM_015650.4:c.1801G>C
MANE Select
|
NP_056465.2:p.Gly601Arg
|
|