ENST00000409709.9:c.5815T=
MANE Select
|
ENSP00000386331.3:p.Ser1939=
|
|
ENST00000670577.1:c.3642T=
|
|
|
ENST00000409619.6:c.5668T=
|
ENSP00000386635.2:p.Ser1890=
|
|
ENST00000409709.7:c.5815T=
|
ENSP00000386331.3:p.Ser1939=
|
|
ENST00000458169.2:c.3241T=
|
ENSP00000417017.2:p.Ser1081=
|
|
ENST00000458637.6:c.5701T=
|
ENSP00000392185.2:p.Ser1901=
|
|
ENST00000481328.7:n.3351T=
|
|
|
ENST00000605744.1:n.729T=
|
|
|
NM_000260.3:c.5815T=
|
NP_000251.3:p.Ser1939=
|
|
NM_001127180.1:c.5701T=
|
NP_001120652.1:p.Ser1901=
|
|
XM_005274012.2:c.5698T=
|
XP_005274069.1:p.Ser1900=
|
|
XM_006718558.2:c.5806T=
|
XP_006718621.1:p.Ser1936=
|
|
XM_006718559.2:c.5701T=
|
XP_006718622.1:p.Ser1901=
|
|
XM_006718560.2:c.5698T=
|
XP_006718623.1:p.Ser1900=
|
|
XM_006718561.2:c.5701T=
|
XP_006718624.1:p.Ser1901=
|
|
XM_011545044.1:c.5815T=
|
XP_011543346.1:p.Ser1939=
|
|
XM_011545045.1:c.5809T=
|
XP_011543347.1:p.Ser1937=
|
|
XM_011545046.1:c.5782T=
|
XP_011543348.1:p.Ser1928=
|
|
XM_011545047.1:c.5719T=
|
XP_011543349.1:p.Ser1907=
|
|
XM_011545048.1:c.5590T=
|
XP_011543350.1:p.Ser1864=
|
|
XM_011545049.1:c.5578T=
|
XP_011543351.1:p.Ser1860=
|
|
XM_011545050.1:c.5551T=
|
XP_011543352.1:p.Ser1851=
|
|
XM_011545051.1:c.5815T=
|
XP_011543353.1:p.Ser1939=
|
|
XR_949938.1:n.6135T=
|
|
|
XR_949941.1:n.6135T=
|
|
|
XM_011545044.2:c.5815T=
|
XP_011543346.1:p.Ser1939=
|
|
XM_011545046.2:c.5905T=
|
XP_011543348.2:p.Ser1969=
|
|
XM_011545050.2:c.5551T=
|
XP_011543352.1:p.Ser1851=
|
|
XM_017017778.1:c.5899T=
|
XP_016873267.1:p.Ser1967=
|
|
XM_017017779.1:c.5896T=
|
XP_016873268.1:p.Ser1966=
|
|
XM_017017780.1:c.5905T=
|
XP_016873269.1:p.Ser1969=
|
|
XM_017017781.1:c.5809T=
|
XP_016873270.1:p.Ser1937=
|
|
XM_017017782.1:c.5791T=
|
XP_016873271.1:p.Ser1931=
|
|
XM_017017783.1:c.5788T=
|
XP_016873272.1:p.Ser1930=
|
|
XM_017017784.1:c.5788T=
|
XP_016873273.1:p.Ser1930=
|
|
XM_017017785.1:c.5668T=
|
XP_016873274.1:p.Ser1890=
|
|
XM_017017786.1:c.5905T=
|
XP_016873275.1:p.Ser1969=
|
|
XM_017017788.1:c.5791T=
|
XP_016873277.1:p.Ser1931=
|
|
XR_001747885.1:n.5920T=
|
|
|
XR_001747886.1:n.5835T=
|
|
|
XR_001747887.1:n.5906T=
|
|
|
NM_000260.4:c.5815T=
MANE Select
|
NP_000251.3:p.Ser1939=
|
|
NM_001127180.2:c.5701T=
|
NP_001120652.1:p.Ser1901=
|
|
NM_001369365.1:c.5668T=
|
NP_001356294.1:p.Ser1890=
|
|