ENST00000322344.8:c.1189-36G>C
MANE Select
|
ENSP00000323511.2:n.1189-36G>C
|
|
ENST00000322344.7:c.1189-36G>C
|
ENSP00000323511.2:n.1189-36G>C
|
|
ENST00000593706.3:n.749G>C
|
|
|
ENST00000593946.5:c.*1116-36G>C
|
ENSP00000468896.1:n.*1116-36G>C
|
|
ENST00000594661.5:n.1690-36G>C
|
|
|
ENST00000596014.5:c.1189-36G>C
|
ENSP00000472300.1:n.1189-36G>C
|
|
ENST00000599454.5:n.33-36G>C
|
|
|
ENST00000600573.5:c.1096-36G>C
|
ENSP00000469826.1:n.1096-36G>C
|
|
ENST00000600910.5:c.1188+127G>C
|
ENSP00000473137.1:n.1188+127G>C
|
|
ENST00000601816.3:n.88-36G>C
|
|
|
ENST00000625216.2:c.270-36G>C
|
ENSP00000486898.1:n.270-36G>C
|
|
ENST00000627232.2:c.1109-36G>C
|
ENSP00000486037.1:n.1109-36G>C
|
|
ENST00000631020.2:c.1081-36G>C
|
ENSP00000486707.1:n.1081-36G>C
|
|
NM_007254.3:c.1189-36G>C
|
NP_009185.2:n.1189-36G>C
|
|
NM_007254.4:c.1189-36G>C
MANE Select
|
NP_009185.2:n.1189-36G>C
|
|