ENST00000584483.6:n.2313A>G
|
|
|
ENST00000697953.1:n.2886A>G
|
|
|
ENST00000698013.1:n.2998A>G
|
|
|
ENST00000698014.1:n.3221A>G
|
|
|
ENST00000698015.1:n.2314A>G
|
|
|
ENST00000698016.1:c.*438A>G
|
ENSP00000513502.1:n.*438A>G
|
|
ENST00000698017.1:n.2388A>G
|
|
|
ENST00000698018.1:n.2519A>G
|
|
|
ENST00000698019.1:n.2717A>G
|
|
|
ENST00000698020.1:n.1823A>G
|
|
|
ENST00000698021.1:c.1732A>G
|
|
|
ENST00000698022.1:c.*438A>G
|
ENSP00000513504.1:n.*438A>G
|
|
ENST00000698023.1:n.2417A>G
|
|
|
ENST00000698024.1:n.2279A>G
|
|
|
ENST00000698025.1:n.2439A>G
|
|
|
ENST00000698026.1:n.1330A>G
|
|
|
ENST00000698027.1:c.*655A>G
|
ENSP00000513505.1:n.*655A>G
|
|
ENST00000698028.1:n.2522A>G
|
|
|
ENST00000698029.1:n.3251A>G
|
|
|
ENST00000448276.7:c.*438A>G
MANE Select
|
ENSP00000392617.2:n.*438A>G
|
|
ENST00000448276.6:c.*438A>G
|
ENSP00000392617.2:n.*438A>G
|
|
ENST00000613943.4:c.1923A>G
|
ENSP00000483605.1:n.1923A>G
|
|
NM_001098426.1:c.*438A>G
|
NP_001091896.1:n.*438A>G
|
|
XM_005257604.2:c.*438A>G
|
XP_005257661.2:n.*438A>G
|
|
NM_001330439.1:c.*438A>G
|
NP_001317368.1:n.*438A>G
|
|
NM_001330440.1:c.*438A>G
|
NP_001317369.1:n.*438A>G
|
|
NM_001098426.2:c.*438A>G
MANE Select
|
NP_001091896.1:n.*438A>G
|
|
NM_001330440.2:c.*438A>G
|
NP_001317369.1:n.*438A>G
|
|