ENST00000276079.13:c.*119G>T
MANE Select
|
ENSP00000276079.8:n.*119G>T
|
|
ENST00000420903.6:c.*119G>T
|
ENSP00000410299.2:n.*119G>T
|
|
ENST00000473525.2:n.2243G>T
|
|
|
ENST00000676495.1:n.2946G>T
|
|
|
ENST00000676499.1:n.2491G>T
|
|
|
ENST00000676797.1:c.*119G>T
|
ENSP00000503920.1:n.*119G>T
|
|
ENST00000677014.1:c.*1362G>T
|
ENSP00000503813.1:n.*1362G>T
|
|
ENST00000677218.1:n.2706G>T
|
|
|
ENST00000677245.1:c.*1744G>T
|
ENSP00000503929.1:n.*1744G>T
|
|
ENST00000677274.1:c.*119G>T
|
ENSP00000504314.1:n.*119G>T
|
|
ENST00000677446.1:c.*119G>T
|
ENSP00000503031.1:n.*119G>T
|
|
ENST00000677612.1:c.*119G>T
|
ENSP00000504351.1:n.*119G>T
|
|
ENST00000677766.1:n.3940G>T
|
|
|
ENST00000677826.1:n.2277G>T
|
|
|
ENST00000677879.1:c.*119G>T
|
ENSP00000504090.1:n.*119G>T
|
|
ENST00000677977.1:n.3367G>T
|
|
|
ENST00000678231.1:c.*119G>T
|
ENSP00000503233.1:n.*119G>T
|
|
ENST00000678323.1:n.2633G>T
|
|
|
ENST00000678335.1:c.*448G>T
|
ENSP00000503769.1:n.*448G>T
|
|
ENST00000678437.1:c.*119G>T
|
ENSP00000504007.1:n.*119G>T
|
|
ENST00000678660.1:c.*119G>T
|
ENSP00000504665.1:n.*119G>T
|
|
ENST00000678830.1:c.*119G>T
|
ENSP00000504263.1:n.*119G>T
|
|
ENST00000679029.1:c.*349G>T
|
ENSP00000504193.1:n.*349G>T
|
|
ENST00000679267.1:n.3742G>T
|
|
|
ENST00000276079.12:c.*119G>T
|
ENSP00000276079.8:n.*119G>T
|
|
ENST00000373841.5:c.*119G>T
|
ENSP00000362947.1:n.*119G>T
|
|
ENST00000373856.7:c.*119G>T
|
ENSP00000362963.3:n.*119G>T
|
|
ENST00000472185.1:n.61-324G>T
|
|
|
ENST00000473525.1:n.1309G>T
|
|
|
ENST00000474431.5:n.570G>T
|
|
|
ENST00000490044.5:n.2242G>T
|
|
|
ENST00000535149.5:c.*119G>T
|
ENSP00000441364.1:n.*119G>T
|
|
NM_001145408.1:c.*119G>T
|
NP_001138880.1:n.*119G>T
|
|
NM_001145409.1:c.*119G>T
|
NP_001138881.1:n.*119G>T
|
|
NM_001145410.1:c.*119G>T
|
NP_001138882.1:n.*119G>T
|
|
NM_007363.4:c.*119G>T
|
NP_031389.3:n.*119G>T
|
|
NM_007363.5:c.*119G>T
MANE Select
|
NP_031389.3:n.*119G>T
|
|
NM_001145408.2:c.*119G>T
|
NP_001138880.1:n.*119G>T
|
|
NM_001145409.2:c.*119G>T
|
NP_001138881.1:n.*119G>T
|
|
NM_001145410.2:c.*119G>T
|
NP_001138882.1:n.*119G>T
|
|