ENST00000467482.6:c.885+179G>C
MANE Select
|
ENSP00000417161.1:n.885+179G>C
|
|
ENST00000447366.5:c.633+179G>C
|
ENSP00000390546.2:n.633+179G>C
|
|
ENST00000467482.5:c.885+179G>C
|
ENSP00000417161.1:n.885+179G>C
|
|
NM_000273.2:c.885+179G>C
|
NP_000264.2:n.885+179G>C
|
|
XM_005274541.2:c.885+179G>C
|
XP_005274598.1:n.885+179G>C
|
|
XM_005274541.3:c.885+179G>C
|
XP_005274598.1:n.885+179G>C
|
|
XM_024452387.1:c.633+179G>C
|
XP_024308155.1:n.633+179G>C
|
|
XM_024452388.1:c.633+179G>C
|
XP_024308156.1:n.633+179G>C
|
|
NM_000273.3:c.885+179G>C
MANE Select
|
NP_000264.2:n.885+179G>C
|
|