ENST00000697953.1:n.3249G>A
|
|
|
ENST00000698013.1:n.3361G>A
|
|
|
ENST00000698014.1:n.3584G>A
|
|
|
ENST00000698015.1:n.2677G>A
|
|
|
ENST00000698016.1:c.*801G>A
|
ENSP00000513502.1:n.*801G>A
|
|
ENST00000698017.1:n.2751G>A
|
|
|
ENST00000698018.1:n.2882G>A
|
|
|
ENST00000698019.1:n.3080G>A
|
|
|
ENST00000698020.1:n.2186G>A
|
|
|
ENST00000698021.1:c.2095G>A
|
|
|
ENST00000698022.1:c.*801G>A
|
ENSP00000513504.1:n.*801G>A
|
|
ENST00000698023.1:n.2780G>A
|
|
|
ENST00000698024.1:n.2642G>A
|
|
|
ENST00000698025.1:n.2802G>A
|
|
|
ENST00000698026.1:n.1693G>A
|
|
|
ENST00000698027.1:c.*1018G>A
|
ENSP00000513505.1:n.*1018G>A
|
|
ENST00000448276.7:c.*801G>A
MANE Select
|
ENSP00000392617.2:n.*801G>A
|
|
ENST00000448276.6:c.*801G>A
|
ENSP00000392617.2:n.*801G>A
|
|
ENST00000613943.4:c.2286G>A
|
ENSP00000483605.1:n.2286G>A
|
|
NM_001098426.1:c.*801G>A
|
NP_001091896.1:n.*801G>A
|
|
XM_005257604.2:c.*801G>A
|
XP_005257661.2:n.*801G>A
|
|
NM_001330439.1:c.*801G>A
|
NP_001317368.1:n.*801G>A
|
|
NM_001330440.1:c.*801G>A
|
NP_001317369.1:n.*801G>A
|
|
NM_001098426.2:c.*801G>A
MANE Select
|
NP_001091896.1:n.*801G>A
|
|
NM_001330440.2:c.*801G>A
|
NP_001317369.1:n.*801G>A
|
|