ENST00000409709.9:c.6033C>T
MANE Select
|
ENSP00000386331.3:p.Ser2011=
|
|
ENST00000670577.1:c.3834C>T
|
|
|
ENST00000409619.6:c.5886C>T
|
ENSP00000386635.2:p.Ser1962=
|
|
ENST00000409709.7:c.6033C>T
|
ENSP00000386331.3:p.Ser2011=
|
|
ENST00000458169.2:c.3459C>T
|
ENSP00000417017.2:p.Ser1153=
|
|
ENST00000458637.6:c.5919C>T
|
ENSP00000392185.2:p.Ser1973=
|
|
ENST00000481328.7:n.3569C>T
|
|
|
ENST00000605744.1:n.947C>T
|
|
|
NM_000260.3:c.6033C>T
|
NP_000251.3:p.Ser2011=
|
|
NM_001127180.1:c.5919C>T
|
NP_001120652.1:p.Ser1973=
|
|
XM_005274012.2:c.5916C>T
|
XP_005274069.1:p.Ser1972=
|
|
XM_006718558.2:c.6024C>T
|
XP_006718621.1:p.Ser2008=
|
|
XM_006718559.2:c.5919C>T
|
XP_006718622.1:p.Ser1973=
|
|
XM_006718560.2:c.5916C>T
|
XP_006718623.1:p.Ser1972=
|
|
XM_006718561.2:c.5919C>T
|
XP_006718624.1:p.Ser1973=
|
|
XM_011545044.1:c.6033C>T
|
XP_011543346.1:p.Ser2011=
|
|
XM_011545045.1:c.6027C>T
|
XP_011543347.1:p.Ser2009=
|
|
XM_011545046.1:c.6000C>T
|
XP_011543348.1:p.Ser2000=
|
|
XM_011545047.1:c.5937C>T
|
XP_011543349.1:p.Ser1979=
|
|
XM_011545048.1:c.5808C>T
|
XP_011543350.1:p.Ser1936=
|
|
XM_011545049.1:c.5796C>T
|
XP_011543351.1:p.Ser1932=
|
|
XM_011545050.1:c.5769C>T
|
XP_011543352.1:p.Ser1923=
|
|
XM_011545051.1:c.6033C>T
|
XP_011543353.1:p.Ser2011=
|
|
XR_949938.1:n.6353C>T
|
|
|
XR_949941.1:n.6327C>T
|
|
|
XM_011545044.2:c.6033C>T
|
XP_011543346.1:p.Ser2011=
|
|
XM_011545046.2:c.6123C>T
|
XP_011543348.2:p.Ser2041=
|
|
XM_011545050.2:c.5769C>T
|
XP_011543352.1:p.Ser1923=
|
|
XM_017017778.1:c.6117C>T
|
XP_016873267.1:p.Ser2039=
|
|
XM_017017779.1:c.6114C>T
|
XP_016873268.1:p.Ser2038=
|
|
XM_017017780.1:c.6123C>T
|
XP_016873269.1:p.Ser2041=
|
|
XM_017017781.1:c.6027C>T
|
XP_016873270.1:p.Ser2009=
|
|
XM_017017782.1:c.6009C>T
|
XP_016873271.1:p.Ser2003=
|
|
XM_017017783.1:c.6006C>T
|
XP_016873272.1:p.Ser2002=
|
|
XM_017017784.1:c.6006C>T
|
XP_016873273.1:p.Ser2002=
|
|
XM_017017785.1:c.5886C>T
|
XP_016873274.1:p.Ser1962=
|
|
XM_017017786.1:c.6123C>T
|
XP_016873275.1:p.Ser2041=
|
|
XM_017017788.1:c.6009C>T
|
XP_016873277.1:p.Ser2003=
|
|
XR_001747885.1:n.6112C>T
|
|
|
XR_001747886.1:n.6053C>T
|
|
|
XR_001747887.1:n.6098C>T
|
|
|
NM_000260.4:c.6033C>T
MANE Select
|
NP_000251.3:p.Ser2011=
|
|
NM_001127180.2:c.5919C>T
|
NP_001120652.1:p.Ser1973=
|
|
NM_001369365.1:c.5886C>T
|
NP_001356294.1:p.Ser1962=
|
|