ENST00000409709.9:c.*156G>T
MANE Select
|
ENSP00000386331.3:n.*156G>T
|
|
ENST00000670577.1:c.4605G>T
|
|
|
ENST00000409619.6:c.*156G>T
|
ENSP00000386635.2:n.*156G>T
|
|
ENST00000409709.7:c.*156G>T
|
ENSP00000386331.3:n.*156G>T
|
|
ENST00000458169.2:c.4230G>T
|
ENSP00000417017.2:n.4230G>T
|
|
ENST00000458637.6:c.*156G>T
|
ENSP00000392185.2:n.*156G>T
|
|
ENST00000481328.7:n.5354G>T
|
|
|
ENST00000605744.1:n.2318G>T
|
|
|
NM_000260.3:c.*156G>T
|
NP_000251.3:n.*156G>T
|
|
NM_001127180.1:c.*156G>T
|
NP_001120652.1:n.*156G>T
|
|
XM_005274012.2:c.*156G>T
|
XP_005274069.1:n.*156G>T
|
|
XM_006718561.2:c.*156G>T
|
XP_006718624.1:n.*156G>T
|
|
XR_949941.1:n.7098G>T
|
|
|
XM_017017780.1:c.*156G>T
|
XP_016873269.1:n.*156G>T
|
|
XM_017017784.1:c.*156G>T
|
XP_016873273.1:n.*156G>T
|
|
XM_017017788.1:c.*156G>T
|
XP_016873277.1:n.*156G>T
|
|
XR_001747885.1:n.6883G>T
|
|
|
XR_001747887.1:n.6869G>T
|
|
|
NM_000260.4:c.*156G>T
MANE Select
|
NP_000251.3:n.*156G>T
|
|
NM_001127180.2:c.*156G>T
|
NP_001120652.1:n.*156G>T
|
|
NM_001369365.1:c.*156G>T
|
NP_001356294.1:n.*156G>T
|
|