ENST00000409709.9:c.*119G>A
MANE Select
|
ENSP00000386331.3:n.*119G>A
|
|
ENST00000670577.1:c.4568G>A
|
|
|
ENST00000409619.6:c.*119G>A
|
ENSP00000386635.2:n.*119G>A
|
|
ENST00000409709.7:c.*119G>A
|
ENSP00000386331.3:n.*119G>A
|
|
ENST00000458169.2:c.4193G>A
|
ENSP00000417017.2:n.4193G>A
|
|
ENST00000458637.6:c.*119G>A
|
ENSP00000392185.2:n.*119G>A
|
|
ENST00000481328.7:n.5317G>A
|
|
|
ENST00000605744.1:n.2281G>A
|
|
|
NM_000260.3:c.*119G>A
|
NP_000251.3:n.*119G>A
|
|
NM_001127180.1:c.*119G>A
|
NP_001120652.1:n.*119G>A
|
|
XM_005274012.2:c.*119G>A
|
XP_005274069.1:n.*119G>A
|
|
XM_006718561.2:c.*119G>A
|
XP_006718624.1:n.*119G>A
|
|
XR_949941.1:n.7061G>A
|
|
|
XM_017017780.1:c.*119G>A
|
XP_016873269.1:n.*119G>A
|
|
XM_017017784.1:c.*119G>A
|
XP_016873273.1:n.*119G>A
|
|
XM_017017788.1:c.*119G>A
|
XP_016873277.1:n.*119G>A
|
|
XR_001747885.1:n.6846G>A
|
|
|
XR_001747887.1:n.6832G>A
|
|
|
NM_000260.4:c.*119G>A
MANE Select
|
NP_000251.3:n.*119G>A
|
|
NM_001127180.2:c.*119G>A
|
NP_001120652.1:n.*119G>A
|
|
NM_001369365.1:c.*119G>A
|
NP_001356294.1:n.*119G>A
|
|