ENST00000584483.6:n.2298T>A
|
|
|
ENST00000697953.1:n.2871T>A
|
|
|
ENST00000698013.1:n.2983T>A
|
|
|
ENST00000698014.1:n.3206T>A
|
|
|
ENST00000698015.1:n.2299T>A
|
|
|
ENST00000698016.1:c.*423T>A
|
ENSP00000513502.1:n.*423T>A
|
|
ENST00000698017.1:n.2373T>A
|
|
|
ENST00000698018.1:n.2504T>A
|
|
|
ENST00000698019.1:n.2702T>A
|
|
|
ENST00000698020.1:n.1808T>A
|
|
|
ENST00000698021.1:c.1717T>A
|
|
|
ENST00000698022.1:c.*423T>A
|
ENSP00000513504.1:n.*423T>A
|
|
ENST00000698023.1:n.2402T>A
|
|
|
ENST00000698024.1:n.2264T>A
|
|
|
ENST00000698025.1:n.2424T>A
|
|
|
ENST00000698026.1:n.1315T>A
|
|
|
ENST00000698027.1:c.*640T>A
|
ENSP00000513505.1:n.*640T>A
|
|
ENST00000698028.1:n.2507T>A
|
|
|
ENST00000698029.1:n.3236T>A
|
|
|
ENST00000448276.7:c.*423T>A
MANE Select
|
ENSP00000392617.2:n.*423T>A
|
|
ENST00000323347.14:c.*423T>A
|
ENSP00000318451.10:n.*423T>A
|
|
ENST00000448276.6:c.*423T>A
|
ENSP00000392617.2:n.*423T>A
|
|
ENST00000613943.4:c.1908T>A
|
ENSP00000483605.1:n.1908T>A
|
|
NM_001098426.1:c.*423T>A
|
NP_001091896.1:n.*423T>A
|
|
XM_005257604.2:c.*423T>A
|
XP_005257661.2:n.*423T>A
|
|
NM_001330439.1:c.*423T>A
|
NP_001317368.1:n.*423T>A
|
|
NM_001330440.1:c.*423T>A
|
NP_001317369.1:n.*423T>A
|
|
NM_001098426.2:c.*423T>A
MANE Select
|
NP_001091896.1:n.*423T>A
|
|
NM_001330440.2:c.*423T>A
|
NP_001317369.1:n.*423T>A
|
|