|
ENST00000261769.10:c.2556G>C
MANE Select
|
ENSP00000261769.4:p.Glu852Asp
|
|
|
ENST00000261769.9:c.2556G>C
|
ENSP00000261769.4:p.Glu852Asp
|
|
|
ENST00000422392.6:c.2373G>C
|
ENSP00000414946.2:p.Glu791Asp
|
|
|
ENST00000562118.1:n.774G>C
|
|
|
|
ENST00000562836.5:n.2627G>C
|
|
|
|
ENST00000566510.5:c.*1222G>C
|
ENSP00000458139.1:n.*1222G>C
|
|
|
ENST00000566612.5:c.*796G>C
|
ENSP00000454782.1:n.*796G>C
|
|
|
ENST00000611625.4:c.2619G>C
|
ENSP00000481063.1:p.Glu873Asp
|
|
|
ENST00000612417.4:c.1854-785G>C
|
ENSP00000478360.1:n.1854-785G>C
|
|
|
ENST00000621016.4:c.1866-797G>C
|
ENSP00000480664.1:n.1866-797G>C
|
|
|
NM_004360.3:c.2556G>C , LRG_301t1:c.2556G>C
|
NP_004351.1:p.Glu852Asp
|
|
|
XM_011523488.1:c.1821G>C
|
XP_011521790.1:p.Glu607Asp
|
|
|
XM_011523489.1:c.1821G>C
|
XP_011521791.1:p.Glu607Asp
|
|
|
NM_001317184.1:c.2373G>C
|
NP_001304113.1:p.Glu791Asp
|
|
|
NM_001317185.1:c.1008G>C
|
NP_001304114.1:p.Glu336Asp
|
|
|
NM_001317186.1:c.591G>C
|
NP_001304115.1:p.Glu197Asp
|
|
|
NM_004360.4:c.2556G>C
|
NP_004351.1:p.Glu852Asp
|
|
|
NM_004360.5:c.2556G>C
MANE Select
|
NP_004351.1:p.Glu852Asp
|
|
|
NM_001317184.2:c.2373G>C
|
NP_001304113.1:p.Glu791Asp
|
|
|
NM_001317185.2:c.1008G>C
|
NP_001304114.1:p.Glu336Asp
|
|
|
NM_001317186.2:c.591G>C
|
NP_001304115.1:p.Glu197Asp
|
|
