ENST00000584483.6:n.2393C>G
|
|
|
ENST00000697953.1:n.2966C>G
|
|
|
ENST00000698013.1:n.3078C>G
|
|
|
ENST00000698014.1:n.3301C>G
|
|
|
ENST00000698015.1:n.2394C>G
|
|
|
ENST00000698016.1:c.*518C>G
|
ENSP00000513502.1:n.*518C>G
|
|
ENST00000698017.1:n.2468C>G
|
|
|
ENST00000698018.1:n.2599C>G
|
|
|
ENST00000698019.1:n.2797C>G
|
|
|
ENST00000698020.1:n.1903C>G
|
|
|
ENST00000698021.1:c.1812C>G
|
|
|
ENST00000698022.1:c.*518C>G
|
ENSP00000513504.1:n.*518C>G
|
|
ENST00000698023.1:n.2497C>G
|
|
|
ENST00000698024.1:n.2359C>G
|
|
|
ENST00000698025.1:n.2519C>G
|
|
|
ENST00000698026.1:n.1410C>G
|
|
|
ENST00000698027.1:c.*735C>G
|
ENSP00000513505.1:n.*735C>G
|
|
ENST00000698028.1:n.2602C>G
|
|
|
ENST00000698029.1:n.3331C>G
|
|
|
ENST00000448276.7:c.*518C>G
MANE Select
|
ENSP00000392617.2:n.*518C>G
|
|
ENST00000448276.6:c.*518C>G
|
ENSP00000392617.2:n.*518C>G
|
|
ENST00000613943.4:c.2003C>G
|
ENSP00000483605.1:n.2003C>G
|
|
NM_001098426.1:c.*518C>G
|
NP_001091896.1:n.*518C>G
|
|
XM_005257604.2:c.*518C>G
|
XP_005257661.2:n.*518C>G
|
|
NM_001330439.1:c.*518C>G
|
NP_001317368.1:n.*518C>G
|
|
NM_001330440.1:c.*518C>G
|
NP_001317369.1:n.*518C>G
|
|
NM_001098426.2:c.*518C>G
MANE Select
|
NP_001091896.1:n.*518C>G
|
|
NM_001330440.2:c.*518C>G
|
NP_001317369.1:n.*518C>G
|
|