|
ENST00000261769.10:c.2603G=
MANE Select
|
ENSP00000261769.4:p.Arg868=
|
|
|
ENST00000261769.9:c.2603G=
|
ENSP00000261769.4:p.Arg868=
|
|
|
ENST00000422392.6:c.2420G=
|
ENSP00000414946.2:p.Arg807=
|
|
|
ENST00000562118.1:n.821G=
|
|
|
|
ENST00000562836.5:n.2674G=
|
|
|
|
ENST00000566510.5:c.*1269G=
|
ENSP00000458139.1:n.*1269G=
|
|
|
ENST00000566612.5:c.*843G=
|
ENSP00000454782.1:n.*843G=
|
|
|
ENST00000611625.4:c.2666G=
|
ENSP00000481063.1:p.Arg889=
|
|
|
ENST00000612417.4:c.1854-738G=
|
ENSP00000478360.1:n.1854-738G=
|
|
|
ENST00000621016.4:c.1866-750G=
|
ENSP00000480664.1:n.1866-750G=
|
|
|
NM_004360.3:c.2603G= , LRG_301t1:c.2603G=
|
NP_004351.1:p.Arg868=
|
|
|
XM_011523488.1:c.1868G=
|
XP_011521790.1:p.Arg623=
|
|
|
XM_011523489.1:c.1868G=
|
XP_011521791.1:p.Arg623=
|
|
|
NM_001317184.1:c.2420G=
|
NP_001304113.1:p.Arg807=
|
|
|
NM_001317185.1:c.1055G=
|
NP_001304114.1:p.Arg352=
|
|
|
NM_001317186.1:c.638G=
|
NP_001304115.1:p.Arg213=
|
|
|
NM_004360.4:c.2603G=
|
NP_004351.1:p.Arg868=
|
|
|
NM_004360.5:c.2603G=
MANE Select
|
NP_004351.1:p.Arg868=
|
|
|
NM_001317184.2:c.2420G=
|
NP_001304113.1:p.Arg807=
|
|
|
NM_001317185.2:c.1055G=
|
NP_001304114.1:p.Arg352=
|
|
|
NM_001317186.2:c.638G=
|
NP_001304115.1:p.Arg213=
|
|
