ENST00000584483.6:n.2507A>C
|
|
|
ENST00000697953.1:n.3080A>C
|
|
|
ENST00000698013.1:n.3192A>C
|
|
|
ENST00000698014.1:n.3415A>C
|
|
|
ENST00000698015.1:n.2508A>C
|
|
|
ENST00000698016.1:c.*632A>C
|
ENSP00000513502.1:n.*632A>C
|
|
ENST00000698017.1:n.2582A>C
|
|
|
ENST00000698018.1:n.2713A>C
|
|
|
ENST00000698019.1:n.2911A>C
|
|
|
ENST00000698020.1:n.2017A>C
|
|
|
ENST00000698021.1:c.1926A>C
|
|
|
ENST00000698022.1:c.*632A>C
|
ENSP00000513504.1:n.*632A>C
|
|
ENST00000698023.1:n.2611A>C
|
|
|
ENST00000698024.1:n.2473A>C
|
|
|
ENST00000698025.1:n.2633A>C
|
|
|
ENST00000698026.1:n.1524A>C
|
|
|
ENST00000698027.1:c.*849A>C
|
ENSP00000513505.1:n.*849A>C
|
|
ENST00000698028.1:n.2716A>C
|
|
|
ENST00000698029.1:n.3445A>C
|
|
|
ENST00000448276.7:c.*632A>C
MANE Select
|
ENSP00000392617.2:n.*632A>C
|
|
ENST00000448276.6:c.*632A>C
|
ENSP00000392617.2:n.*632A>C
|
|
ENST00000613943.4:c.2117A>C
|
ENSP00000483605.1:n.2117A>C
|
|
NM_001098426.1:c.*632A>C
|
NP_001091896.1:n.*632A>C
|
|
XM_005257604.2:c.*632A>C
|
XP_005257661.2:n.*632A>C
|
|
NM_001330439.1:c.*632A>C
|
NP_001317368.1:n.*632A>C
|
|
NM_001330440.1:c.*632A>C
|
NP_001317369.1:n.*632A>C
|
|
NM_001098426.2:c.*632A>C
MANE Select
|
NP_001091896.1:n.*632A>C
|
|
NM_001330440.2:c.*632A>C
|
NP_001317369.1:n.*632A>C
|
|