ENST00000697149.1:c.1634G>C
|
ENSP00000513138.1:n.1634G>C
|
|
ENST00000697150.1:c.1692G>C
|
ENSP00000513139.1:n.1692G>C
|
|
ENST00000697151.1:c.1625G>C
|
ENSP00000513140.1:n.1625G>C
|
|
ENST00000697164.1:c.1705G>C
|
ENSP00000513153.1:p.Gly569Arg
|
|
ENST00000697165.1:c.1492G>C
|
ENSP00000513154.1:p.Gly498Arg
|
|
ENST00000347310.10:c.1795G>C
MANE Select
|
ENSP00000321345.5:p.Gly599Arg
|
|
ENST00000637002.1:c.1186G>C
|
ENSP00000490340.1:p.Gly396Arg
|
|
ENST00000347310.9:c.1795G>C
|
ENSP00000321345.5:p.Gly599Arg
|
|
ENST00000395227.2:c.589G>C
|
ENSP00000378652.2:p.Gly197Arg
|
|
ENST00000425614.3:c.1030G>C
|
ENSP00000387640.2:p.Gly344Arg
|
|
ENST00000473881.2:c.*621G>C
|
ENSP00000486667.1:n.*621G>C
|
|
NM_144701.2:c.1795G>C
|
NP_653302.2:p.Gly599Arg
|
|
XM_005270516.2:c.1033G>C
|
XP_005270573.1:p.Gly345Arg
|
|
XM_011540789.1:c.1885G>C
|
XP_011539091.1:p.Gly629Arg
|
|
XM_011540790.1:c.1795G>C
|
XP_011539092.1:p.Gly599Arg
|
|
XM_011540791.1:c.1795G>C
|
XP_011539093.1:p.Gly599Arg
|
|
XM_011540790.3:c.1795G>C
|
XP_011539092.1:p.Gly599Arg
|
|
XM_011540791.3:c.1795G>C
|
XP_011539093.1:p.Gly599Arg
|
|
XR_001736993.1:n.1875G>C
|
|
|
NM_144701.3:c.1795G>C
MANE Select
|
NP_653302.2:p.Gly599Arg
|
|