ENST00000262367.10:c.5296G>A
MANE Select
|
ENSP00000262367.5:p.Glu1766Lys
|
|
ENST00000262367.9:c.5296G>A
|
ENSP00000262367.5:p.Glu1766Lys
|
|
ENST00000382070.7:c.5182G>A
|
ENSP00000371502.3:p.Glu1728Lys
|
|
NM_001079846.1:c.5182G>A
|
NP_001073315.1:p.Glu1728Lys
|
|
NM_004380.2:c.5296G>A
|
NP_004371.2:p.Glu1766Lys
|
|
XM_005255124.3:c.5251G>A
|
XP_005255181.1:p.Glu1751Lys
|
|
XM_005255125.3:c.4879G>A
|
XP_005255182.1:p.Glu1627Lys
|
|
XM_006720848.2:c.5035G>A
|
XP_006720911.1:p.Glu1679Lys
|
|
XM_011522380.1:c.5242G>A
|
XP_011520682.1:p.Glu1748Lys
|
|
XM_011522381.1:c.4543G>A
|
XP_011520683.1:p.Glu1515Lys
|
|
XM_005255124.4:c.5251G>A
|
XP_005255181.1:p.Glu1751Lys
|
|
XM_005255125.4:c.4879G>A
|
XP_005255182.1:p.Glu1627Lys
|
|
XM_006720848.3:c.5035G>A
|
XP_006720911.1:p.Glu1679Lys
|
|
XM_011522381.2:c.4543G>A
|
XP_011520683.1:p.Glu1515Lys
|
|
XM_017022944.1:c.5290G>A
|
XP_016878433.1:p.Glu1764Lys
|
|
NM_004380.3:c.5296G>A
MANE Select
|
NP_004371.2:p.Glu1766Lys
|
|