ENST00000468990.2:c.*190G>C
|
ENSP00000512215.1:n.*190G>C
|
|
ENST00000494324.2:c.*454G>C
|
ENSP00000512216.1:n.*454G>C
|
|
ENST00000695842.1:c.349G>C
|
ENSP00000512214.1:p.Gly117Arg
|
|
ENST00000695843.1:c.*190G>C
|
ENSP00000512217.1:n.*190G>C
|
|
ENST00000696144.1:c.349G>C
|
ENSP00000512436.1:p.Gly117Arg
|
|
ENST00000696164.1:c.349G>C
|
ENSP00000512454.1:p.Gly117Arg
|
|
ENST00000696165.1:c.*190G>C
|
ENSP00000512455.1:n.*190G>C
|
|
ENST00000696166.1:c.*190G>C
|
ENSP00000512456.1:n.*190G>C
|
|
ENST00000371237.9:c.349G>C
MANE Select
|
ENSP00000360281.4:p.Gly117Arg
|
|
ENST00000371237.8:c.349G>C
|
ENSP00000360281.4:p.Gly117Arg
|
|
ENST00000535057.5:c.163G>C
|
ENSP00000440113.1:p.Gly55Arg
|
|
ENST00000543257.5:c.193G>C
|
ENSP00000442548.1:p.Gly65Arg
|
|
XM_017002235.1:c.349G>C
|
XP_016857724.1:p.Gly117Arg
|
|
XR_001737397.1:n.449G>C
|
|
|
NM_000066.4:c.349G>C
MANE Select
|
NP_000057.3:p.Gly117Arg
|
|
NM_001278543.2:c.193G>C
|
NP_001265472.2:p.Gly65Arg
|
|
NM_001278544.2:c.163G>C
|
NP_001265473.2:p.Gly55Arg
|
|