ENST00000322344.8:c.1399A>C
MANE Select
|
ENSP00000323511.2:p.Thr467Pro
|
|
ENST00000636840.1:c.59+110A>C
|
|
|
ENST00000640501.1:c.5A>C
|
|
|
ENST00000322344.7:c.1399A>C
|
ENSP00000323511.2:p.Thr467Pro
|
|
ENST00000593946.5:c.*1326A>C
|
ENSP00000468896.1:n.*1326A>C
|
|
ENST00000594661.5:n.1900A>C
|
|
|
ENST00000595081.5:n.302A>C
|
|
|
ENST00000596014.5:c.1399A>C
|
ENSP00000472300.1:p.Thr467Pro
|
|
ENST00000597965.2:c.106A>C
|
ENSP00000471097.2:p.Thr36Pro
|
|
ENST00000599454.5:n.319A>C
|
|
|
ENST00000600573.5:c.1306A>C
|
ENSP00000469826.1:p.Thr436Pro
|
|
ENST00000600910.5:c.1289A>C
|
ENSP00000473137.1:p.Asp430Ala
|
|
ENST00000601816.3:n.471A>C
|
|
|
ENST00000625216.2:c.480A>C
|
ENSP00000486898.1:n.480A>C
|
|
ENST00000627232.2:c.1319A>C
|
ENSP00000486037.1:n.1319A>C
|
|
ENST00000631020.2:c.1291A>C
|
ENSP00000486707.1:p.Thr431Pro
|
|
NM_007254.3:c.1399A>C
|
NP_009185.2:p.Thr467Pro
|
|
NM_007254.4:c.1399A>C
MANE Select
|
NP_009185.2:p.Thr467Pro
|
|