ENST00000642683.1:c.622G>C
|
ENSP00000495376.1:p.Gly208Arg
|
|
ENST00000643672.1:c.619G>C
|
ENSP00000494532.1:p.Gly207Arg
|
|
ENST00000645280.1:c.616G>C
|
ENSP00000496690.1:p.Gly206Arg
|
|
ENST00000648579.1:c.726G>C
|
ENSP00000497638.1:p.Val242=
|
|
ENST00000650617.1:c.670G>C
MANE Select
|
ENSP00000497532.1:p.Gly224Arg
|
|
ENST00000273158.8:c.670G>C
|
ENSP00000273158.3:p.Gly224Arg
|
|
NM_017875.2:c.670G>C
|
NP_060345.2:p.Gly224Arg
|
|
XM_006713214.1:c.658G>C
|
XP_006713277.1:p.Gly220Arg
|
|
XM_011533869.1:c.652G>C
|
XP_011532171.1:p.Gly218Arg
|
|
XM_011533870.1:c.619G>C
|
XP_011532172.1:p.Gly207Arg
|
|
XM_011533871.1:c.490G>C
|
XP_011532173.1:p.Gly164Arg
|
|
NM_001354798.1:c.626-1944G>C
|
NP_001341727.1:n.626-1944G>C
|
|
NM_017875.4:c.670G>C
MANE Select
|
NP_060345.2:p.Gly224Arg
|
|
XM_006713214.2:c.658G>C
|
XP_006713277.1:p.Gly220Arg
|
|
XM_011533869.2:c.652G>C
|
XP_011532171.1:p.Gly218Arg
|
|
XM_024453611.1:c.616G>C
|
XP_024309379.1:p.Gly206Arg
|
|
NM_001354798.2:c.626-1944G>C
|
NP_001341727.1:n.626-1944G>C
|
|