ENST00000366577.10:c.1817G>T
MANE Select
|
ENSP00000355536.5:p.Gly606Val
|
|
ENST00000535889.6:c.1817G>T
|
ENSP00000441845.1:p.Gly606Val
|
|
ENST00000650888.1:c.*859G>T
|
ENSP00000498393.1:n.*859G>T
|
|
ENST00000651455.1:c.*561G>T
|
ENSP00000498963.1:n.*561G>T
|
|
ENST00000674797.2:c.1469G>T
|
ENSP00000502299.2:p.Gly490Val
|
|
ENST00000679569.1:n.2131G>T
|
|
|
ENST00000679842.1:c.1817G>T
|
ENSP00000506109.1:p.Gly606Val
|
|
ENST00000680454.1:n.2261G>T
|
|
|
ENST00000681102.1:c.1637G>T
|
ENSP00000505600.1:p.Gly546Val
|
|
ENST00000681177.1:c.1516-6881G>T
|
ENSP00000506327.1:n.1516-6881G>T
|
|
ENST00000681937.1:n.2148-6881G>T
|
|
|
ENST00000366576.3:c.479G>T
|
ENSP00000355535.3:p.Gly160Val
|
|
ENST00000366577.9:c.1817G>T
|
ENSP00000355536.5:p.Gly606Val
|
|
ENST00000463959.1:n.1836G>T
|
|
|
ENST00000535889.5:c.1817G>T
|
ENSP00000441845.1:p.Gly606Val
|
|
NM_000254.2:c.1817G>T
|
NP_000245.2:p.Gly606Val
|
|
NM_001291939.1:c.1817G>T
|
NP_001278868.1:p.Gly606Val
|
|
NM_001291940.1:c.596G>T
|
NP_001278869.1:p.Gly199Val
|
|
XM_005273141.3:c.1814G>T
|
XP_005273198.1:p.Gly605Val
|
|
XM_006711769.2:c.1817G>T
|
XP_006711832.1:p.Gly606Val
|
|
XM_006711770.1:c.881G>T
|
XP_006711833.1:p.Gly294Val
|
|
XM_011544193.1:c.1817G>T
|
XP_011542495.1:p.Gly606Val
|
|
XM_011544194.1:c.1985G>T
|
XP_011542496.1:p.Gly662Val
|
|
XM_005273141.5:c.1814G>T
|
XP_005273198.1:p.Gly605Val
|
|
XM_006711770.3:c.881G>T
|
XP_006711833.1:p.Gly294Val
|
|
XM_011544194.3:c.1985G>T
|
XP_011542496.1:p.Gly662Val
|
|
XM_017001329.2:c.1985G>T
|
XP_016856818.1:p.Gly662Val
|
|
XM_017001330.2:c.1985G>T
|
XP_016856819.1:p.Gly662Val
|
|
NM_001291940.2:c.596G>T
|
NP_001278869.1:p.Gly199Val
|
|
NM_000254.3:c.1817G>T
MANE Select
|
NP_000245.2:p.Gly606Val
|
|