ENST00000601549.2:n.1151-487T>A
|
|
|
ENST00000648053.1:n.552-487T>A
|
|
|
ENST00000648319.1:c.1120-487T>A
MANE Select
|
ENSP00000496939.1:n.1120-487T>A
|
|
ENST00000262888.7:c.1120-487T>A
|
ENSP00000262888.3:n.1120-487T>A
|
|
ENST00000597184.5:n.196-487T>A
|
|
|
ENST00000598836.1:c.332-487T>A
|
|
|
ENST00000599720.5:c.*390-487T>A
|
ENSP00000472513.1:n.*390-487T>A
|
|
ENST00000600408.1:c.518-487T>A
|
ENSP00000472510.1:n.518-487T>A
|
|
ENST00000600909.1:c.16-487T>A
|
ENSP00000470339.1:n.16-487T>A
|
|
ENST00000601549.1:n.838-487T>A
|
|
|
ENST00000615047.4:c.724-487T>A
|
ENSP00000485014.1:n.724-487T>A
|
|
NM_002250.2:c.1120-487T>A
|
NP_002241.1:n.1120-487T>A
|
|
XM_005258882.2:c.1024-487T>A
|
XP_005258939.1:n.1024-487T>A
|
|
XM_005258883.2:c.931-487T>A
|
XP_005258940.1:n.931-487T>A
|
|
XR_935823.1:n.2366-487T>A
|
|
|
XR_002958313.1:n.2512-487T>A
|
|
|
NM_002250.3:c.1120-487T>A
MANE Select
|
NP_002241.1:n.1120-487T>A
|
|