ENST00000584483.6:n.2461T>C
|
|
|
ENST00000697953.1:n.3034T>C
|
|
|
ENST00000698013.1:n.3146T>C
|
|
|
ENST00000698014.1:n.3369T>C
|
|
|
ENST00000698015.1:n.2462T>C
|
|
|
ENST00000698016.1:c.*586T>C
|
ENSP00000513502.1:n.*586T>C
|
|
ENST00000698017.1:n.2536T>C
|
|
|
ENST00000698018.1:n.2667T>C
|
|
|
ENST00000698019.1:n.2865T>C
|
|
|
ENST00000698020.1:n.1971T>C
|
|
|
ENST00000698021.1:c.1880T>C
|
|
|
ENST00000698022.1:c.*586T>C
|
ENSP00000513504.1:n.*586T>C
|
|
ENST00000698023.1:n.2565T>C
|
|
|
ENST00000698024.1:n.2427T>C
|
|
|
ENST00000698025.1:n.2587T>C
|
|
|
ENST00000698026.1:n.1478T>C
|
|
|
ENST00000698027.1:c.*803T>C
|
ENSP00000513505.1:n.*803T>C
|
|
ENST00000698028.1:n.2670T>C
|
|
|
ENST00000698029.1:n.3399T>C
|
|
|
ENST00000448276.7:c.*586T>C
MANE Select
|
ENSP00000392617.2:n.*586T>C
|
|
ENST00000448276.6:c.*586T>C
|
ENSP00000392617.2:n.*586T>C
|
|
ENST00000613943.4:c.2071T>C
|
ENSP00000483605.1:n.2071T>C
|
|
NM_001098426.1:c.*586T>C
|
NP_001091896.1:n.*586T>C
|
|
XM_005257604.2:c.*586T>C
|
XP_005257661.2:n.*586T>C
|
|
NM_001330439.1:c.*586T>C
|
NP_001317368.1:n.*586T>C
|
|
NM_001330440.1:c.*586T>C
|
NP_001317369.1:n.*586T>C
|
|
NM_001098426.2:c.*586T>C
MANE Select
|
NP_001091896.1:n.*586T>C
|
|
NM_001330440.2:c.*586T>C
|
NP_001317369.1:n.*586T>C
|
|