ENST00000584483.6:n.2627G>T
|
|
|
ENST00000697953.1:n.3200G>T
|
|
|
ENST00000698013.1:n.3312G>T
|
|
|
ENST00000698014.1:n.3535G>T
|
|
|
ENST00000698015.1:n.2628G>T
|
|
|
ENST00000698016.1:c.*752G>T
|
ENSP00000513502.1:n.*752G>T
|
|
ENST00000698017.1:n.2702G>T
|
|
|
ENST00000698018.1:n.2833G>T
|
|
|
ENST00000698019.1:n.3031G>T
|
|
|
ENST00000698020.1:n.2137G>T
|
|
|
ENST00000698021.1:c.2046G>T
|
|
|
ENST00000698022.1:c.*752G>T
|
ENSP00000513504.1:n.*752G>T
|
|
ENST00000698023.1:n.2731G>T
|
|
|
ENST00000698024.1:n.2593G>T
|
|
|
ENST00000698025.1:n.2753G>T
|
|
|
ENST00000698026.1:n.1644G>T
|
|
|
ENST00000698027.1:c.*969G>T
|
ENSP00000513505.1:n.*969G>T
|
|
ENST00000698028.1:n.2836G>T
|
|
|
ENST00000448276.7:c.*752G>T
MANE Select
|
ENSP00000392617.2:n.*752G>T
|
|
ENST00000448276.6:c.*752G>T
|
ENSP00000392617.2:n.*752G>T
|
|
ENST00000613943.4:c.2237G>T
|
ENSP00000483605.1:n.2237G>T
|
|
NM_001098426.1:c.*752G>T
|
NP_001091896.1:n.*752G>T
|
|
XM_005257604.2:c.*752G>T
|
XP_005257661.2:n.*752G>T
|
|
NM_001330439.1:c.*752G>T
|
NP_001317368.1:n.*752G>T
|
|
NM_001330440.1:c.*752G>T
|
NP_001317369.1:n.*752G>T
|
|
NM_001098426.2:c.*752G>T
MANE Select
|
NP_001091896.1:n.*752G>T
|
|
NM_001330440.2:c.*752G>T
|
NP_001317369.1:n.*752G>T
|
|