|
NM_001379200.1:c.955G=
MANE Select
|
NP_001366129.1:p.Gly319=
|
|
ENST00000649276.2:c.955G=
MANE Select
|
ENSP00000497003.1:p.Gly319=
|
|
NM_005992.1:c.928G=
|
NP_005983.1:p.Gly310=
|
|
NM_080646.1:c.928G=
|
NP_542377.1:p.Gly310=
|
|
NM_080646.2:c.928G=
|
NP_542377.1:p.Gly310=
|
|
NM_080647.1:c.928G= , LRG_226t1:c.928G=
|
NP_542378.1:p.Gly310=
|
|
ENST00000329705.11:c.928G=
|
ENSP00000331176.7:p.Gly310=
|
|
ENST00000332710.8:c.928G=
|
ENSP00000331791.4:p.Gly310=
|
|
ENST00000359500.7:c.928G=
|
ENSP00000352483.3:p.Gly310=
|
|
ENST00000484336.1:n.123G=
|
|
|
ENST00000621939.1:c.928G=
|
ENSP00000477982.1:p.Gly310=
|
|
ENST00000700274.1:c.481G=
|
ENSP00000514909.1:p.Gly161=
|
|
XM_006724312.1:c.928G=
|
XP_006724375.1:p.Gly310=
|
|
XM_006724312.2:c.928G=
|
XP_006724375.1:p.Gly310=
|
|
XM_011530351.1:c.955G=
|
XP_011528653.1:p.Gly319=
|
|
XM_017028925.1:c.1078G=
|
XP_016884414.1:p.Gly360=
|
|
XM_017028926.1:c.928G=
|
XP_016884415.1:p.Gly310=
|
|
XM_017028927.1:c.283G=
|
XP_016884416.1:p.Gly95=
|
|
XM_017028928.1:c.1078G=
|
XP_016884417.1:p.Gly360=
|