ENST00000261769.10:c.1491G>C
MANE Select
|
ENSP00000261769.4:p.Glu497Asp
|
|
ENST00000261769.9:c.1491G>C
|
ENSP00000261769.4:p.Glu497Asp
|
|
ENST00000422392.6:c.1308G>C
|
ENSP00000414946.2:p.Glu436Asp
|
|
ENST00000562836.5:n.1562G>C
|
|
|
ENST00000566510.5:c.*157G>C
|
ENSP00000458139.1:n.*157G>C
|
|
ENST00000566612.5:c.1491G>C
|
ENSP00000454782.1:p.Glu497Asp
|
|
ENST00000611625.4:c.1554G>C
|
ENSP00000481063.1:p.Glu518Asp
|
|
ENST00000612417.4:c.1491G>C
|
ENSP00000478360.1:p.Glu497Asp
|
|
ENST00000621016.4:c.1491G>C
|
ENSP00000480664.1:p.Glu497Asp
|
|
NM_004360.3:c.1491G>C , LRG_301t1:c.1491G>C
|
NP_004351.1:p.Glu497Asp
|
|
XM_011523488.1:c.756G>C
|
XP_011521790.1:p.Glu252Asp
|
|
XM_011523489.1:c.756G>C
|
XP_011521791.1:p.Glu252Asp
|
|
NM_001317184.1:c.1308G>C
|
NP_001304113.1:p.Glu436Asp
|
|
NM_001317185.1:c.-58G>C
|
NP_001304114.1:n.-58G>C
|
|
NM_001317186.1:c.-329G>C
|
NP_001304115.1:n.-329G>C
|
|
NM_004360.4:c.1491G>C
|
NP_004351.1:p.Glu497Asp
|
|
NM_004360.5:c.1491G>C
MANE Select
|
NP_004351.1:p.Glu497Asp
|
|
NM_001317184.2:c.1308G>C
|
NP_001304113.1:p.Glu436Asp
|
|
NM_001317185.2:c.-58G>C
|
NP_001304114.1:n.-58G>C
|
|
NM_001317186.2:c.-329G>C
|
NP_001304115.1:n.-329G>C
|
|