ENST00000276079.13:c.1325A>T
MANE Select
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ENSP00000276079.8:p.Glu442Val
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ENST00000373856.8:c.1423A>T
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ENSP00000362963.4:p.Lys475Ter
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ENST00000420903.6:c.1325A>T
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ENSP00000410299.2:p.Glu442Val
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ENST00000450092.6:c.1325A>T
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ENSP00000415777.2:p.Glu442Val
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ENST00000454976.2:c.1325A>T
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ENSP00000406673.2:p.Glu442Val
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ENST00000473525.2:n.2033A>T
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ENST00000676495.1:n.2736A>T
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ENST00000676499.1:n.2281A>T
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ENST00000676797.1:c.1058A>T
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ENSP00000503920.1:p.Glu353Val
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ENST00000677014.1:c.*1152A>T
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ENSP00000503813.1:n.*1152A>T
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ENST00000677218.1:n.2496A>T
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|
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ENST00000677245.1:c.*1534A>T
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ENSP00000503929.1:n.*1534A>T
|
|
ENST00000677274.1:c.1325A>T
|
ENSP00000504314.1:p.Glu442Val
|
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ENST00000677446.1:c.1325A>T
|
ENSP00000503031.1:p.Glu442Val
|
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ENST00000677612.1:c.1325A>T
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ENSP00000504351.1:p.Glu442Val
|
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ENST00000677766.1:n.3730A>T
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|
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ENST00000677826.1:n.2067A>T
|
|
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ENST00000677879.1:c.1145A>T
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ENSP00000504090.1:p.Glu382Val
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ENST00000677977.1:n.3157A>T
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|
|
ENST00000678231.1:c.1325A>T
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ENSP00000503233.1:p.Glu442Val
|
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ENST00000678323.1:n.2423A>T
|
|
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ENST00000678335.1:c.*238A>T
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ENSP00000503769.1:n.*238A>T
|
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ENST00000678437.1:c.1316A>T
|
ENSP00000504007.1:p.Glu439Val
|
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ENST00000678660.1:c.1340A>T
|
ENSP00000504665.1:p.Glu447Val
|
|
ENST00000678830.1:c.1415A>T
|
ENSP00000504263.1:p.Glu472Val
|
|
ENST00000679029.1:c.*139A>T
|
ENSP00000504193.1:n.*139A>T
|
|
ENST00000679267.1:n.3532A>T
|
|
|
ENST00000276079.12:c.1325A>T
|
ENSP00000276079.8:p.Glu442Val
|
|
ENST00000373841.5:c.1325A>T
|
ENSP00000362947.1:p.Glu442Val
|
|
ENST00000373856.7:c.1325A>T
|
ENSP00000362963.3:p.Glu442Val
|
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ENST00000472185.1:n.61-534A>T
|
|
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ENST00000473525.1:n.1099A>T
|
|
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ENST00000474431.5:n.360A>T
|
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ENST00000490044.5:n.2032A>T
|
|
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ENST00000535149.5:c.1058A>T
|
ENSP00000441364.1:p.Glu353Val
|
|
NM_001145408.1:c.1325A>T
|
NP_001138880.1:p.Glu442Val
|
|
NM_001145409.1:c.1325A>T
|
NP_001138881.1:p.Glu442Val
|
|
NM_001145410.1:c.1058A>T
|
NP_001138882.1:p.Glu353Val
|
|
NM_007363.4:c.1325A>T
|
NP_031389.3:p.Glu442Val
|
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NM_007363.5:c.1325A>T
MANE Select
|
NP_031389.3:p.Glu442Val
|
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NM_001145408.2:c.1325A>T
|
NP_001138880.1:p.Glu442Val
|
|
NM_001145409.2:c.1325A>T
|
NP_001138881.1:p.Glu442Val
|
|
NM_001145410.2:c.1058A>T
|
NP_001138882.1:p.Glu353Val
|
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