ENST00000261769.10:c.1428T>G
MANE Select
|
ENSP00000261769.4:p.Asp476Glu
|
|
ENST00000261769.9:c.1428T>G
|
ENSP00000261769.4:p.Asp476Glu
|
|
ENST00000422392.6:c.1245T>G
|
ENSP00000414946.2:p.Asp415Glu
|
|
ENST00000562836.5:n.1499T>G
|
|
|
ENST00000566510.5:c.*94T>G
|
ENSP00000458139.1:n.*94T>G
|
|
ENST00000566612.5:c.1428T>G
|
ENSP00000454782.1:p.Asp476Glu
|
|
ENST00000611625.4:c.1491T>G
|
ENSP00000481063.1:p.Asp497Glu
|
|
ENST00000612417.4:c.1428T>G
|
ENSP00000478360.1:p.Asp476Glu
|
|
ENST00000621016.4:c.1428T>G
|
ENSP00000480664.1:p.Asp476Glu
|
|
NM_004360.3:c.1428T>G , LRG_301t1:c.1428T>G
|
NP_004351.1:p.Asp476Glu
|
|
XM_011523488.1:c.693T>G
|
XP_011521790.1:p.Asp231Glu
|
|
XM_011523489.1:c.693T>G
|
XP_011521791.1:p.Asp231Glu
|
|
NM_001317184.1:c.1245T>G
|
NP_001304113.1:p.Asp415Glu
|
|
NM_001317185.1:c.-121T>G
|
NP_001304114.1:n.-121T>G
|
|
NM_001317186.1:c.-392T>G
|
NP_001304115.1:n.-392T>G
|
|
NM_004360.4:c.1428T>G
|
NP_004351.1:p.Asp476Glu
|
|
NM_004360.5:c.1428T>G
MANE Select
|
NP_004351.1:p.Asp476Glu
|
|
NM_001317184.2:c.1245T>G
|
NP_001304113.1:p.Asp415Glu
|
|
NM_001317185.2:c.-121T>G
|
NP_001304114.1:n.-121T>G
|
|
NM_001317186.2:c.-392T>G
|
NP_001304115.1:n.-392T>G
|
|