|
ENST00000261769.10:c.2640G>A
MANE Select
|
ENSP00000261769.4:p.Glu880=
|
|
|
ENST00000261769.9:c.2640G>A
|
ENSP00000261769.4:p.Glu880=
|
|
|
ENST00000422392.6:c.2457G>A
|
ENSP00000414946.2:p.Glu819=
|
|
|
ENST00000562118.1:n.858G>A
|
|
|
|
ENST00000562836.5:n.2711G>A
|
|
|
|
ENST00000566510.5:c.*1306G>A
|
ENSP00000458139.1:n.*1306G>A
|
|
|
ENST00000566612.5:c.*880G>A
|
ENSP00000454782.1:n.*880G>A
|
|
|
ENST00000611625.4:c.2703G>A
|
ENSP00000481063.1:p.Glu901=
|
|
|
ENST00000612417.4:c.1854-701G>A
|
ENSP00000478360.1:n.1854-701G>A
|
|
|
ENST00000621016.4:c.1866-713G>A
|
ENSP00000480664.1:n.1866-713G>A
|
|
|
NM_004360.3:c.2640G>A , LRG_301t1:c.2640G>A
|
NP_004351.1:p.Glu880=
|
|
|
XM_011523488.1:c.1905G>A
|
XP_011521790.1:p.Glu635=
|
|
|
XM_011523489.1:c.1905G>A
|
XP_011521791.1:p.Glu635=
|
|
|
NM_001317184.1:c.2457G>A
|
NP_001304113.1:p.Glu819=
|
|
|
NM_001317185.1:c.1092G>A
|
NP_001304114.1:p.Glu364=
|
|
|
NM_001317186.1:c.675G>A
|
NP_001304115.1:p.Glu225=
|
|
|
NM_004360.4:c.2640G>A
|
NP_004351.1:p.Glu880=
|
|
|
NM_004360.5:c.2640G>A
MANE Select
|
NP_004351.1:p.Glu880=
|
|
|
NM_001317184.2:c.2457G>A
|
NP_001304113.1:p.Glu819=
|
|
|
NM_001317185.2:c.1092G>A
|
NP_001304114.1:p.Glu364=
|
|
|
NM_001317186.2:c.675G>A
|
NP_001304115.1:p.Glu225=
|
|
