ENST00000262367.10:c.5895G>C
MANE Select
|
ENSP00000262367.5:p.Glu1965Asp
|
|
ENST00000262367.9:c.5895G>C
|
ENSP00000262367.5:p.Glu1965Asp
|
|
ENST00000382070.7:c.5781G>C
|
ENSP00000371502.3:p.Glu1927Asp
|
|
NM_001079846.1:c.5781G>C
|
NP_001073315.1:p.Glu1927Asp
|
|
NM_004380.2:c.5895G>C
|
NP_004371.2:p.Glu1965Asp
|
|
XM_005255124.3:c.5850G>C
|
XP_005255181.1:p.Glu1950Asp
|
|
XM_005255125.3:c.5478G>C
|
XP_005255182.1:p.Glu1826Asp
|
|
XM_006720848.2:c.5634G>C
|
XP_006720911.1:p.Glu1878Asp
|
|
XM_011522380.1:c.5841G>C
|
XP_011520682.1:p.Glu1947Asp
|
|
XM_011522381.1:c.5142G>C
|
XP_011520683.1:p.Glu1714Asp
|
|
XM_005255124.4:c.5850G>C
|
XP_005255181.1:p.Glu1950Asp
|
|
XM_005255125.4:c.5478G>C
|
XP_005255182.1:p.Glu1826Asp
|
|
XM_006720848.3:c.5634G>C
|
XP_006720911.1:p.Glu1878Asp
|
|
XM_011522381.2:c.5142G>C
|
XP_011520683.1:p.Glu1714Asp
|
|
XM_017022944.1:c.5889G>C
|
XP_016878433.1:p.Glu1963Asp
|
|
NM_004380.3:c.5895G>C
MANE Select
|
NP_004371.2:p.Glu1965Asp
|
|