ENST00000409709.9:c.4765G>C
MANE Select
|
ENSP00000386331.3:p.Asp1589His
|
|
ENST00000670577.1:c.2606G>C
|
|
|
ENST00000409619.6:c.4618G>C
|
ENSP00000386635.2:p.Asp1540His
|
|
ENST00000409709.7:c.4765G>C
|
ENSP00000386331.3:p.Asp1589His
|
|
ENST00000458169.2:c.2194G>C
|
ENSP00000417017.2:p.Asp732His
|
|
ENST00000458637.6:c.4651G>C
|
ENSP00000392185.2:p.Asp1551His
|
|
ENST00000481328.7:n.2304G>C
|
|
|
NM_000260.3:c.4765G>C
|
NP_000251.3:p.Asp1589His
|
|
NM_001127180.1:c.4651G>C
|
NP_001120652.1:p.Asp1551His
|
|
XM_005274012.2:c.4651G>C
|
XP_005274069.1:p.Asp1551His
|
|
XM_006718558.2:c.4759G>C
|
XP_006718621.1:p.Asp1587His
|
|
XM_006718559.2:c.4651G>C
|
XP_006718622.1:p.Asp1551His
|
|
XM_006718560.2:c.4651G>C
|
XP_006718623.1:p.Asp1551His
|
|
XM_006718561.2:c.4651G>C
|
XP_006718624.1:p.Asp1551His
|
|
XM_011545044.1:c.4765G>C
|
XP_011543346.1:p.Asp1589His
|
|
XM_011545045.1:c.4759G>C
|
XP_011543347.1:p.Asp1587His
|
|
XM_011545046.1:c.4732G>C
|
XP_011543348.1:p.Asp1578His
|
|
XM_011545047.1:c.4669G>C
|
XP_011543349.1:p.Asp1557His
|
|
XM_011545048.1:c.4540G>C
|
XP_011543350.1:p.Asp1514His
|
|
XM_011545049.1:c.4528G>C
|
XP_011543351.1:p.Asp1510His
|
|
XM_011545050.1:c.4501G>C
|
XP_011543352.1:p.Asp1501His
|
|
XM_011545051.1:c.4765G>C
|
XP_011543353.1:p.Asp1589His
|
|
XM_011545052.1:c.4765G>C
|
XP_011543354.1:p.Asp1589His
|
|
XR_949938.1:n.5085G>C
|
|
|
XR_949941.1:n.5085G>C
|
|
|
XR_949942.1:n.5087G>C
|
|
|
XM_011545044.2:c.4765G>C
|
XP_011543346.1:p.Asp1589His
|
|
XM_011545046.2:c.4855G>C
|
XP_011543348.2:p.Asp1619His
|
|
XM_011545050.2:c.4501G>C
|
XP_011543352.1:p.Asp1501His
|
|
XM_017017778.1:c.4849G>C
|
XP_016873267.1:p.Asp1617His
|
|
XM_017017779.1:c.4849G>C
|
XP_016873268.1:p.Asp1617His
|
|
XM_017017780.1:c.4855G>C
|
XP_016873269.1:p.Asp1619His
|
|
XM_017017781.1:c.4759G>C
|
XP_016873270.1:p.Asp1587His
|
|
XM_017017782.1:c.4741G>C
|
XP_016873271.1:p.Asp1581His
|
|
XM_017017783.1:c.4741G>C
|
XP_016873272.1:p.Asp1581His
|
|
XM_017017784.1:c.4741G>C
|
XP_016873273.1:p.Asp1581His
|
|
XM_017017785.1:c.4618G>C
|
XP_016873274.1:p.Asp1540His
|
|
XM_017017786.1:c.4855G>C
|
XP_016873275.1:p.Asp1619His
|
|
XM_017017788.1:c.4741G>C
|
XP_016873277.1:p.Asp1581His
|
|
XR_001747885.1:n.4870G>C
|
|
|
XR_001747886.1:n.4870G>C
|
|
|
XR_001747887.1:n.4870G>C
|
|
|
XR_001747888.1:n.4870G>C
|
|
|
NM_000260.4:c.4765G>C
MANE Select
|
NP_000251.3:p.Asp1589His
|
|
NM_001127180.2:c.4651G>C
|
NP_001120652.1:p.Asp1551His
|
|
NM_001369365.1:c.4618G>C
|
NP_001356294.1:p.Asp1540His
|
|