ENST00000242152.7:c.*132C>A
MANE Select
|
ENSP00000242152.2:n.*132C>A
|
|
ENST00000242152.6:c.*132C>A
|
ENSP00000242152.2:n.*132C>A
|
|
ENST00000405982.1:c.*132C>A
|
ENSP00000385282.1:n.*132C>A
|
|
NM_000905.3:c.*132C>A
|
NP_000896.1:n.*132C>A
|
|
XM_017012910.1:c.41+27538G>T
|
XP_016868399.1:n.41+27538G>T
|
|
XM_017012911.1:c.41+27538G>T
|
XP_016868400.1:n.41+27538G>T
|
|
XR_001745121.1:n.473+27538G>T
|
|
|
XR_001745122.1:n.345-94790G>T
|
|
|
XR_001745123.1:n.473+27538G>T
|
|
|
XR_001745124.1:n.473+27538G>T
|
|
|
XR_001745125.1:n.473+27538G>T
|
|
|
XR_001745126.1:n.473+27538G>T
|
|
|
XR_001745127.1:n.345-36120G>T
|
|
|
XR_001745129.1:n.473+27538G>T
|
|
|
XR_001745130.1:n.473+27538G>T
|
|
|
XR_001745131.1:n.473+27538G>T
|
|
|
XR_001745132.1:n.473+27538G>T
|
|
|
NM_000905.4:c.*132C>A
MANE Select
|
NP_000896.1:n.*132C>A
|
|