ENST00000456935.7:c.160-7T>C
MANE Select
|
ENSP00000395473.2:n.160-7T>C
|
|
ENST00000221363.8:c.160-7T>C
|
ENSP00000221363.4:n.160-7T>C
|
|
ENST00000456935.6:c.160-7T>C
|
ENSP00000395473.2:n.160-7T>C
|
|
ENST00000466794.5:n.142-7T>C
|
|
|
ENST00000486847.2:c.160-287T>C
|
ENSP00000470174.1:n.160-287T>C
|
|
ENST00000596512.5:n.201-287T>C
|
|
|
ENST00000597961.1:c.151-7T>C
|
ENSP00000472710.1:n.151-7T>C
|
|
ENST00000598876.1:c.180T>C
|
ENSP00000470533.1:p.Pro60=
|
|
ENST00000600281.1:n.201-7T>C
|
|
|
NM_000528.3:c.160-7T>C
|
NP_000519.2:n.160-7T>C
|
|
NM_001173498.1:c.160-7T>C
|
NP_001166969.1:n.160-7T>C
|
|
XM_005259913.1:c.160-7T>C
|
XP_005259970.1:n.160-7T>C
|
|
XM_005259913.2:c.160-7T>C
|
XP_005259970.1:n.160-7T>C
|
|
XM_024451518.1:c.-859-7T>C
|
XP_024307286.1:n.-859-7T>C
|
|
NM_000528.4:c.160-7T>C
MANE Select
|
NP_000519.2:n.160-7T>C
|
|
NM_001173498.2:c.160-7T>C
|
NP_001166969.1:n.160-7T>C
|
|