ENST00000366577.10:c.2769T>G
MANE Select
|
ENSP00000355536.5:p.Ser923=
|
|
ENST00000535889.6:c.2616T>G
|
ENSP00000441845.1:p.Ser872=
|
|
ENST00000650888.1:c.*1811T>G
|
ENSP00000498393.1:n.*1811T>G
|
|
ENST00000651455.1:c.*1513T>G
|
ENSP00000498963.1:n.*1513T>G
|
|
ENST00000674797.2:c.2421T>G
|
ENSP00000502299.2:p.Ser807=
|
|
ENST00000679569.1:n.3083T>G
|
|
|
ENST00000679842.1:c.2580T>G
|
ENSP00000506109.1:p.Ser860=
|
|
ENST00000680454.1:n.3213T>G
|
|
|
ENST00000681102.1:c.2589T>G
|
ENSP00000505600.1:p.Ser863=
|
|
ENST00000681177.1:c.2331T>G
|
ENSP00000506327.1:p.Ser777=
|
|
ENST00000681937.1:n.2963T>G
|
|
|
ENST00000366576.3:c.1431T>G
|
ENSP00000355535.3:p.Ser477=
|
|
ENST00000366577.9:c.2769T>G
|
ENSP00000355536.5:p.Ser923=
|
|
ENST00000535889.5:c.2616T>G
|
ENSP00000441845.1:p.Ser872=
|
|
NM_000254.2:c.2769T>G
|
NP_000245.2:p.Ser923=
|
|
NM_001291939.1:c.2616T>G
|
NP_001278868.1:p.Ser872=
|
|
NM_001291940.1:c.1548T>G
|
NP_001278869.1:p.Ser516=
|
|
XM_005273141.3:c.2766T>G
|
XP_005273198.1:p.Ser922=
|
|
XM_006711769.2:c.2769T>G
|
XP_006711832.1:p.Ser923=
|
|
XM_006711770.1:c.1833T>G
|
XP_006711833.1:p.Ser611=
|
|
XM_011544193.1:c.2580T>G
|
XP_011542495.1:p.Ser860=
|
|
XM_011544194.1:c.2937T>G
|
XP_011542496.1:p.Ser979=
|
|
XM_005273141.5:c.2766T>G
|
XP_005273198.1:p.Ser922=
|
|
XM_006711770.3:c.1833T>G
|
XP_006711833.1:p.Ser611=
|
|
XM_011544194.3:c.2937T>G
|
XP_011542496.1:p.Ser979=
|
|
XM_017001329.2:c.2784T>G
|
XP_016856818.1:p.Ser928=
|
|
XM_017001330.2:c.2748T>G
|
XP_016856819.1:p.Ser916=
|
|
NM_001291940.2:c.1548T>G
|
NP_001278869.1:p.Ser516=
|
|
NM_000254.3:c.2769T>G
MANE Select
|
NP_000245.2:p.Ser923=
|
|