ENST00000276079.13:c.*116C>T
MANE Select
|
ENSP00000276079.8:n.*116C>T
|
|
ENST00000420903.6:c.*116C>T
|
ENSP00000410299.2:n.*116C>T
|
|
ENST00000473525.2:n.2240C>T
|
|
|
ENST00000676495.1:n.2943C>T
|
|
|
ENST00000676499.1:n.2488C>T
|
|
|
ENST00000676797.1:c.*116C>T
|
ENSP00000503920.1:n.*116C>T
|
|
ENST00000677014.1:c.*1359C>T
|
ENSP00000503813.1:n.*1359C>T
|
|
ENST00000677218.1:n.2703C>T
|
|
|
ENST00000677245.1:c.*1741C>T
|
ENSP00000503929.1:n.*1741C>T
|
|
ENST00000677274.1:c.*116C>T
|
ENSP00000504314.1:n.*116C>T
|
|
ENST00000677446.1:c.*116C>T
|
ENSP00000503031.1:n.*116C>T
|
|
ENST00000677612.1:c.*116C>T
|
ENSP00000504351.1:n.*116C>T
|
|
ENST00000677766.1:n.3937C>T
|
|
|
ENST00000677826.1:n.2274C>T
|
|
|
ENST00000677879.1:c.*116C>T
|
ENSP00000504090.1:n.*116C>T
|
|
ENST00000677977.1:n.3364C>T
|
|
|
ENST00000678231.1:c.*116C>T
|
ENSP00000503233.1:n.*116C>T
|
|
ENST00000678323.1:n.2630C>T
|
|
|
ENST00000678335.1:c.*445C>T
|
ENSP00000503769.1:n.*445C>T
|
|
ENST00000678437.1:c.*116C>T
|
ENSP00000504007.1:n.*116C>T
|
|
ENST00000678660.1:c.*116C>T
|
ENSP00000504665.1:n.*116C>T
|
|
ENST00000678830.1:c.*116C>T
|
ENSP00000504263.1:n.*116C>T
|
|
ENST00000679029.1:c.*346C>T
|
ENSP00000504193.1:n.*346C>T
|
|
ENST00000679267.1:n.3739C>T
|
|
|
ENST00000276079.12:c.*116C>T
|
ENSP00000276079.8:n.*116C>T
|
|
ENST00000373841.5:c.*116C>T
|
ENSP00000362947.1:n.*116C>T
|
|
ENST00000373856.7:c.*116C>T
|
ENSP00000362963.3:n.*116C>T
|
|
ENST00000472185.1:n.61-327C>T
|
|
|
ENST00000473525.1:n.1306C>T
|
|
|
ENST00000474431.5:n.567C>T
|
|
|
ENST00000490044.5:n.2239C>T
|
|
|
ENST00000535149.5:c.*116C>T
|
ENSP00000441364.1:n.*116C>T
|
|
NM_001145408.1:c.*116C>T
|
NP_001138880.1:n.*116C>T
|
|
NM_001145409.1:c.*116C>T
|
NP_001138881.1:n.*116C>T
|
|
NM_001145410.1:c.*116C>T
|
NP_001138882.1:n.*116C>T
|
|
NM_007363.4:c.*116C>T
|
NP_031389.3:n.*116C>T
|
|
NM_007363.5:c.*116C>T
MANE Select
|
NP_031389.3:n.*116C>T
|
|
NM_001145408.2:c.*116C>T
|
NP_001138880.1:n.*116C>T
|
|
NM_001145409.2:c.*116C>T
|
NP_001138881.1:n.*116C>T
|
|
NM_001145410.2:c.*116C>T
|
NP_001138882.1:n.*116C>T
|
|