ENST00000584483.6:n.2285T>G
|
|
|
ENST00000697953.1:n.2858T>G
|
|
|
ENST00000698013.1:n.2970T>G
|
|
|
ENST00000698014.1:n.3193T>G
|
|
|
ENST00000698015.1:n.2286T>G
|
|
|
ENST00000698016.1:c.*410T>G
|
ENSP00000513502.1:n.*410T>G
|
|
ENST00000698017.1:n.2360T>G
|
|
|
ENST00000698018.1:n.2491T>G
|
|
|
ENST00000698019.1:n.2689T>G
|
|
|
ENST00000698020.1:n.1795T>G
|
|
|
ENST00000698021.1:c.1704T>G
|
|
|
ENST00000698022.1:c.*410T>G
|
ENSP00000513504.1:n.*410T>G
|
|
ENST00000698023.1:n.2389T>G
|
|
|
ENST00000698024.1:n.2251T>G
|
|
|
ENST00000698025.1:n.2411T>G
|
|
|
ENST00000698026.1:n.1302T>G
|
|
|
ENST00000698027.1:c.*627T>G
|
ENSP00000513505.1:n.*627T>G
|
|
ENST00000698028.1:n.2494T>G
|
|
|
ENST00000698029.1:n.3223T>G
|
|
|
ENST00000448276.7:c.*410T>G
MANE Select
|
ENSP00000392617.2:n.*410T>G
|
|
ENST00000323347.14:c.*410T>G
|
ENSP00000318451.10:n.*410T>G
|
|
ENST00000448276.6:c.*410T>G
|
ENSP00000392617.2:n.*410T>G
|
|
ENST00000613943.4:c.1895T>G
|
ENSP00000483605.1:n.1895T>G
|
|
NM_001098426.1:c.*410T>G
|
NP_001091896.1:n.*410T>G
|
|
XM_005257604.2:c.*410T>G
|
XP_005257661.2:n.*410T>G
|
|
NM_001330439.1:c.*410T>G
|
NP_001317368.1:n.*410T>G
|
|
NM_001330440.1:c.*410T>G
|
NP_001317369.1:n.*410T>G
|
|
NM_001098426.2:c.*410T>G
MANE Select
|
NP_001091896.1:n.*410T>G
|
|
NM_001330440.2:c.*410T>G
|
NP_001317369.1:n.*410T>G
|
|