ENST00000366577.10:c.1780A>G
MANE Select
|
ENSP00000355536.5:p.Met594Val
|
|
ENST00000535889.6:c.1780A>G
|
ENSP00000441845.1:p.Met594Val
|
|
ENST00000650888.1:c.*822A>G
|
ENSP00000498393.1:n.*822A>G
|
|
ENST00000651455.1:c.*524A>G
|
ENSP00000498963.1:n.*524A>G
|
|
ENST00000674797.2:c.1432A>G
|
ENSP00000502299.2:p.Met478Val
|
|
ENST00000679569.1:n.2094A>G
|
|
|
ENST00000679842.1:c.1780A>G
|
ENSP00000506109.1:p.Met594Val
|
|
ENST00000680454.1:n.2224A>G
|
|
|
ENST00000681102.1:c.1600A>G
|
ENSP00000505600.1:p.Met534Val
|
|
ENST00000681177.1:c.1516-7228A>G
|
ENSP00000506327.1:n.1516-7228A>G
|
|
ENST00000681937.1:n.2148-7228A>G
|
|
|
ENST00000366576.3:c.442A>G
|
ENSP00000355535.3:p.Met148Val
|
|
ENST00000366577.9:c.1780A>G
|
ENSP00000355536.5:p.Met594Val
|
|
ENST00000463959.1:n.1799A>G
|
|
|
ENST00000535889.5:c.1780A>G
|
ENSP00000441845.1:p.Met594Val
|
|
NM_000254.2:c.1780A>G
|
NP_000245.2:p.Met594Val
|
|
NM_001291939.1:c.1780A>G
|
NP_001278868.1:p.Met594Val
|
|
NM_001291940.1:c.559A>G
|
NP_001278869.1:p.Met187Val
|
|
XM_005273141.3:c.1777A>G
|
XP_005273198.1:p.Met593Val
|
|
XM_006711769.2:c.1780A>G
|
XP_006711832.1:p.Met594Val
|
|
XM_006711770.1:c.844A>G
|
XP_006711833.1:p.Met282Val
|
|
XM_011544193.1:c.1780A>G
|
XP_011542495.1:p.Met594Val
|
|
XM_011544194.1:c.1948A>G
|
XP_011542496.1:p.Met650Val
|
|
XM_005273141.5:c.1777A>G
|
XP_005273198.1:p.Met593Val
|
|
XM_006711770.3:c.844A>G
|
XP_006711833.1:p.Met282Val
|
|
XM_011544194.3:c.1948A>G
|
XP_011542496.1:p.Met650Val
|
|
XM_017001329.2:c.1948A>G
|
XP_016856818.1:p.Met650Val
|
|
XM_017001330.2:c.1948A>G
|
XP_016856819.1:p.Met650Val
|
|
NM_001291940.2:c.559A>G
|
NP_001278869.1:p.Met187Val
|
|
NM_000254.3:c.1780A>G
MANE Select
|
NP_000245.2:p.Met594Val
|
|