ENST00000276079.13:c.1320A>T
MANE Select
|
ENSP00000276079.8:p.Thr440=
|
|
ENST00000373856.8:c.1418A>T
|
ENSP00000362963.4:p.Gln473Leu
|
|
ENST00000420903.6:c.1320A>T
|
ENSP00000410299.2:p.Thr440=
|
|
ENST00000450092.6:c.1320A>T
|
ENSP00000415777.2:p.Thr440=
|
|
ENST00000454976.2:c.1320A>T
|
ENSP00000406673.2:p.Thr440=
|
|
ENST00000473525.2:n.2028A>T
|
|
|
ENST00000676495.1:n.2731A>T
|
|
|
ENST00000676499.1:n.2276A>T
|
|
|
ENST00000676797.1:c.1053A>T
|
ENSP00000503920.1:p.Thr351=
|
|
ENST00000677014.1:c.*1147A>T
|
ENSP00000503813.1:n.*1147A>T
|
|
ENST00000677218.1:n.2491A>T
|
|
|
ENST00000677245.1:c.*1529A>T
|
ENSP00000503929.1:n.*1529A>T
|
|
ENST00000677274.1:c.1320A>T
|
ENSP00000504314.1:p.Thr440=
|
|
ENST00000677446.1:c.1320A>T
|
ENSP00000503031.1:p.Thr440=
|
|
ENST00000677612.1:c.1320A>T
|
ENSP00000504351.1:p.Thr440=
|
|
ENST00000677766.1:n.3725A>T
|
|
|
ENST00000677826.1:n.2062A>T
|
|
|
ENST00000677879.1:c.1140A>T
|
ENSP00000504090.1:p.Thr380=
|
|
ENST00000677977.1:n.3152A>T
|
|
|
ENST00000678231.1:c.1320A>T
|
ENSP00000503233.1:p.Thr440=
|
|
ENST00000678323.1:n.2418A>T
|
|
|
ENST00000678335.1:c.*233A>T
|
ENSP00000503769.1:n.*233A>T
|
|
ENST00000678437.1:c.1311A>T
|
ENSP00000504007.1:p.Thr437=
|
|
ENST00000678660.1:c.1335A>T
|
ENSP00000504665.1:p.Thr445=
|
|
ENST00000678830.1:c.1410A>T
|
ENSP00000504263.1:p.Thr470=
|
|
ENST00000679029.1:c.*134A>T
|
ENSP00000504193.1:n.*134A>T
|
|
ENST00000679267.1:n.3527A>T
|
|
|
ENST00000276079.12:c.1320A>T
|
ENSP00000276079.8:p.Thr440=
|
|
ENST00000373841.5:c.1320A>T
|
ENSP00000362947.1:p.Thr440=
|
|
ENST00000373856.7:c.1320A>T
|
ENSP00000362963.3:p.Thr440=
|
|
ENST00000472185.1:n.61-539A>T
|
|
|
ENST00000473525.1:n.1094A>T
|
|
|
ENST00000474431.5:n.355A>T
|
|
|
ENST00000490044.5:n.2027A>T
|
|
|
ENST00000535149.5:c.1053A>T
|
ENSP00000441364.1:p.Thr351=
|
|
NM_001145408.1:c.1320A>T
|
NP_001138880.1:p.Thr440=
|
|
NM_001145409.1:c.1320A>T
|
NP_001138881.1:p.Thr440=
|
|
NM_001145410.1:c.1053A>T
|
NP_001138882.1:p.Thr351=
|
|
NM_007363.4:c.1320A>T
|
NP_031389.3:p.Thr440=
|
|
NM_007363.5:c.1320A>T
MANE Select
|
NP_031389.3:p.Thr440=
|
|
NM_001145408.2:c.1320A>T
|
NP_001138880.1:p.Thr440=
|
|
NM_001145409.2:c.1320A>T
|
NP_001138881.1:p.Thr440=
|
|
NM_001145410.2:c.1053A>T
|
NP_001138882.1:p.Thr351=
|
|