ENST00000584483.6:n.2591T>C
|
|
|
ENST00000697953.1:n.3164T>C
|
|
|
ENST00000698013.1:n.3276T>C
|
|
|
ENST00000698014.1:n.3499T>C
|
|
|
ENST00000698015.1:n.2592T>C
|
|
|
ENST00000698016.1:c.*716T>C
|
ENSP00000513502.1:n.*716T>C
|
|
ENST00000698017.1:n.2666T>C
|
|
|
ENST00000698018.1:n.2797T>C
|
|
|
ENST00000698019.1:n.2995T>C
|
|
|
ENST00000698020.1:n.2101T>C
|
|
|
ENST00000698021.1:c.2010T>C
|
|
|
ENST00000698022.1:c.*716T>C
|
ENSP00000513504.1:n.*716T>C
|
|
ENST00000698023.1:n.2695T>C
|
|
|
ENST00000698024.1:n.2557T>C
|
|
|
ENST00000698025.1:n.2717T>C
|
|
|
ENST00000698026.1:n.1608T>C
|
|
|
ENST00000698027.1:c.*933T>C
|
ENSP00000513505.1:n.*933T>C
|
|
ENST00000698028.1:n.2800T>C
|
|
|
ENST00000448276.7:c.*716T>C
MANE Select
|
ENSP00000392617.2:n.*716T>C
|
|
ENST00000448276.6:c.*716T>C
|
ENSP00000392617.2:n.*716T>C
|
|
ENST00000613943.4:c.2201T>C
|
ENSP00000483605.1:n.2201T>C
|
|
NM_001098426.1:c.*716T>C
|
NP_001091896.1:n.*716T>C
|
|
XM_005257604.2:c.*716T>C
|
XP_005257661.2:n.*716T>C
|
|
NM_001330439.1:c.*716T>C
|
NP_001317368.1:n.*716T>C
|
|
NM_001330440.1:c.*716T>C
|
NP_001317369.1:n.*716T>C
|
|
NM_001098426.2:c.*716T>C
MANE Select
|
NP_001091896.1:n.*716T>C
|
|
NM_001330440.2:c.*716T>C
|
NP_001317369.1:n.*716T>C
|
|