ENST00000409709.9:c.5968C=
MANE Select
|
ENSP00000386331.3:p.Gln1990=
|
|
ENST00000670577.1:c.3772-3C=
|
|
|
ENST00000409619.6:c.5821C=
|
ENSP00000386635.2:p.Gln1941=
|
|
ENST00000409709.7:c.5968C=
|
ENSP00000386331.3:p.Gln1990=
|
|
ENST00000458169.2:c.3394C=
|
ENSP00000417017.2:p.Gln1132=
|
|
ENST00000458637.6:c.5854C=
|
ENSP00000392185.2:p.Gln1952=
|
|
ENST00000481328.7:n.3504C=
|
|
|
ENST00000605744.1:n.882C=
|
|
|
NM_000260.3:c.5968C=
|
NP_000251.3:p.Gln1990=
|
|
NM_001127180.1:c.5854C=
|
NP_001120652.1:p.Gln1952=
|
|
XM_005274012.2:c.5851C=
|
XP_005274069.1:p.Gln1951=
|
|
XM_006718558.2:c.5959C=
|
XP_006718621.1:p.Gln1987=
|
|
XM_006718559.2:c.5854C=
|
XP_006718622.1:p.Gln1952=
|
|
XM_006718560.2:c.5851C=
|
XP_006718623.1:p.Gln1951=
|
|
XM_006718561.2:c.5854C=
|
XP_006718624.1:p.Gln1952=
|
|
XM_011545044.1:c.5968C=
|
XP_011543346.1:p.Gln1990=
|
|
XM_011545045.1:c.5962C=
|
XP_011543347.1:p.Gln1988=
|
|
XM_011545046.1:c.5935C=
|
XP_011543348.1:p.Gln1979=
|
|
XM_011545047.1:c.5872C=
|
XP_011543349.1:p.Gln1958=
|
|
XM_011545048.1:c.5743C=
|
XP_011543350.1:p.Gln1915=
|
|
XM_011545049.1:c.5731C=
|
XP_011543351.1:p.Gln1911=
|
|
XM_011545050.1:c.5704C=
|
XP_011543352.1:p.Gln1902=
|
|
XM_011545051.1:c.5968C=
|
XP_011543353.1:p.Gln1990=
|
|
XR_949938.1:n.6288C=
|
|
|
XR_949941.1:n.6265-3C=
|
|
|
XM_011545044.2:c.5968C=
|
XP_011543346.1:p.Gln1990=
|
|
XM_011545046.2:c.6058C=
|
XP_011543348.2:p.Gln2020=
|
|
XM_011545050.2:c.5704C=
|
XP_011543352.1:p.Gln1902=
|
|
XM_017017778.1:c.6052C=
|
XP_016873267.1:p.Gln2018=
|
|
XM_017017779.1:c.6049C=
|
XP_016873268.1:p.Gln2017=
|
|
XM_017017780.1:c.6058C=
|
XP_016873269.1:p.Gln2020=
|
|
XM_017017781.1:c.5962C=
|
XP_016873270.1:p.Gln1988=
|
|
XM_017017782.1:c.5944C=
|
XP_016873271.1:p.Gln1982=
|
|
XM_017017783.1:c.5941C=
|
XP_016873272.1:p.Gln1981=
|
|
XM_017017784.1:c.5941C=
|
XP_016873273.1:p.Gln1981=
|
|
XM_017017785.1:c.5821C=
|
XP_016873274.1:p.Gln1941=
|
|
XM_017017786.1:c.6058C=
|
XP_016873275.1:p.Gln2020=
|
|
XM_017017788.1:c.5944C=
|
XP_016873277.1:p.Gln1982=
|
|
XR_001747885.1:n.6050-3C=
|
|
|
XR_001747886.1:n.5988C=
|
|
|
XR_001747887.1:n.6036-3C=
|
|
|
NM_000260.4:c.5968C=
MANE Select
|
NP_000251.3:p.Gln1990=
|
|
NM_001127180.2:c.5854C=
|
NP_001120652.1:p.Gln1952=
|
|
NM_001369365.1:c.5821C=
|
NP_001356294.1:p.Gln1941=
|
|