ENST00000584483.6:n.2467T>C
|
|
|
ENST00000697953.1:n.3040T>C
|
|
|
ENST00000698013.1:n.3152T>C
|
|
|
ENST00000698014.1:n.3375T>C
|
|
|
ENST00000698015.1:n.2468T>C
|
|
|
ENST00000698016.1:c.*592T>C
|
ENSP00000513502.1:n.*592T>C
|
|
ENST00000698017.1:n.2542T>C
|
|
|
ENST00000698018.1:n.2673T>C
|
|
|
ENST00000698019.1:n.2871T>C
|
|
|
ENST00000698020.1:n.1977T>C
|
|
|
ENST00000698021.1:c.1886T>C
|
|
|
ENST00000698022.1:c.*592T>C
|
ENSP00000513504.1:n.*592T>C
|
|
ENST00000698023.1:n.2571T>C
|
|
|
ENST00000698024.1:n.2433T>C
|
|
|
ENST00000698025.1:n.2593T>C
|
|
|
ENST00000698026.1:n.1484T>C
|
|
|
ENST00000698027.1:c.*809T>C
|
ENSP00000513505.1:n.*809T>C
|
|
ENST00000698028.1:n.2676T>C
|
|
|
ENST00000698029.1:n.3405T>C
|
|
|
ENST00000448276.7:c.*592T>C
MANE Select
|
ENSP00000392617.2:n.*592T>C
|
|
ENST00000448276.6:c.*592T>C
|
ENSP00000392617.2:n.*592T>C
|
|
ENST00000613943.4:c.2077T>C
|
ENSP00000483605.1:n.2077T>C
|
|
NM_001098426.1:c.*592T>C
|
NP_001091896.1:n.*592T>C
|
|
XM_005257604.2:c.*592T>C
|
XP_005257661.2:n.*592T>C
|
|
NM_001330439.1:c.*592T>C
|
NP_001317368.1:n.*592T>C
|
|
NM_001330440.1:c.*592T>C
|
NP_001317369.1:n.*592T>C
|
|
NM_001098426.2:c.*592T>C
MANE Select
|
NP_001091896.1:n.*592T>C
|
|
NM_001330440.2:c.*592T>C
|
NP_001317369.1:n.*592T>C
|
|