ENST00000460843.6:c.1994G>A
MANE Select
|
ENSP00000417980.1:p.Gly665Asp
|
|
ENST00000636027.1:c.1880G>A
|
ENSP00000489961.1:p.Gly627Asp
|
|
ENST00000637161.1:c.1901G>A
|
ENSP00000490328.1:p.Gly634Asp
|
|
ENST00000637261.1:c.2034G>A
|
ENSP00000490815.1:n.2034G>A
|
|
ENST00000638071.1:c.1621G>A
|
|
|
ENST00000640639.1:c.1163G>A
|
ENSP00000491823.1:p.Gly388Asp
|
|
ENST00000371394.6:c.*1729G>A
|
ENSP00000485945.1:n.*1729G>A
|
|
ENST00000460843.5:c.1994G>A
|
ENSP00000417980.1:p.Gly665Asp
|
|
ENST00000462484.5:c.1994G>A
|
ENSP00000417328.1:p.Gly665Asp
|
|
ENST00000462942.3:c.851G>A
|
ENSP00000436107.1:p.Gly284Asp
|
|
ENST00000626603.1:n.1629C>T
|
|
|
NM_001145527.1:c.1994G>A
|
NP_001138999.1:p.Gly665Asp
|
|
NM_024757.4:c.1994G>A
|
NP_079033.4:p.Gly665Asp
|
|
XM_005266105.3:c.1985G>A
|
XP_005266162.1:p.Gly662Asp
|
|
XM_005266110.1:c.1901G>A
|
XP_005266167.1:p.Gly634Asp
|
|
XM_006717288.2:c.1976G>A
|
XP_006717351.1:p.Gly659Asp
|
|
XM_011519021.1:c.2003G>A
|
XP_011517323.1:p.Gly668Asp
|
|
XM_011519022.1:c.2000G>A
|
XP_011517324.1:p.Gly667Asp
|
|
XM_011519023.1:c.1982G>A
|
XP_011517325.1:p.Gly661Asp
|
|
XM_011519024.1:c.1925G>A
|
XP_011517326.1:p.Gly642Asp
|
|
XM_011519025.1:c.1901G>A
|
XP_011517327.1:p.Gly634Asp
|
|
XM_011519026.1:c.1859G>A
|
XP_011517328.1:p.Gly620Asp
|
|
XM_011519027.1:c.2003G>A
|
XP_011517329.1:p.Gly668Asp
|
|
XM_011519028.1:c.2003G>A
|
XP_011517330.1:p.Gly668Asp
|
|
XM_011519029.1:c.425G>A
|
XP_011517331.1:p.Gly142Asp
|
|
XM_011519033.1:c.1838G>A
|
XP_011517335.1:p.Gly613Asp
|
|
NM_001354259.1:c.1901G>A
|
NP_001341188.1:p.Gly634Asp
|
|
NM_001354263.1:c.1973G>A
|
NP_001341192.1:p.Gly658Asp
|
|
XM_005266105.5:c.1985G>A
|
XP_005266162.1:p.Gly662Asp
|
|
XM_011519021.3:c.2003G>A
|
XP_011517323.1:p.Gly668Asp
|
|
XM_011519022.3:c.2000G>A
|
XP_011517324.1:p.Gly667Asp
|
|
XM_011519023.3:c.1982G>A
|
XP_011517325.1:p.Gly661Asp
|
|
XM_011519029.3:c.425G>A
|
XP_011517331.1:p.Gly142Asp
|
|
XM_017015134.1:c.1979G>A
|
XP_016870623.1:p.Gly660Asp
|
|
XM_017015136.2:c.1895G>A
|
XP_016870625.1:p.Gly632Asp
|
|
XM_017015137.1:c.1880G>A
|
XP_016870626.1:p.Gly627Asp
|
|
XM_017015138.1:c.1880G>A
|
XP_016870627.1:p.Gly627Asp
|
|
XM_024447674.1:c.1823G>A
|
XP_024303442.1:p.Gly608Asp
|
|
XM_024447675.1:c.1757G>A
|
XP_024303443.1:p.Gly586Asp
|
|
XM_024447676.1:c.1118G>A
|
XP_024303444.1:p.Gly373Asp
|
|
XM_024447677.1:c.1118G>A
|
XP_024303445.1:p.Gly373Asp
|
|
XM_024447678.1:c.1901G>A
|
XP_024303446.1:p.Gly634Asp
|
|
XM_024447679.1:c.1901G>A
|
XP_024303447.1:p.Gly634Asp
|
|
XM_024447680.1:c.1736G>A
|
XP_024303448.1:p.Gly579Asp
|
|
NM_024757.5:c.1994G>A
MANE Select
|
NP_079033.4:p.Gly665Asp
|
|
NM_001145527.2:c.1994G>A
|
NP_001138999.1:p.Gly665Asp
|
|
NM_001354259.2:c.1901G>A
|
NP_001341188.1:p.Gly634Asp
|
|
NM_001354263.2:c.1973G>A
|
NP_001341192.1:p.Gly658Asp
|
|