ENST00000584483.6:n.2319G>T
|
|
|
ENST00000697953.1:n.2892G>T
|
|
|
ENST00000698013.1:n.3004G>T
|
|
|
ENST00000698014.1:n.3227G>T
|
|
|
ENST00000698015.1:n.2320G>T
|
|
|
ENST00000698016.1:c.*444G>T
|
ENSP00000513502.1:n.*444G>T
|
|
ENST00000698017.1:n.2394G>T
|
|
|
ENST00000698018.1:n.2525G>T
|
|
|
ENST00000698019.1:n.2723G>T
|
|
|
ENST00000698020.1:n.1829G>T
|
|
|
ENST00000698021.1:c.1738G>T
|
|
|
ENST00000698022.1:c.*444G>T
|
ENSP00000513504.1:n.*444G>T
|
|
ENST00000698023.1:n.2423G>T
|
|
|
ENST00000698024.1:n.2285G>T
|
|
|
ENST00000698025.1:n.2445G>T
|
|
|
ENST00000698026.1:n.1336G>T
|
|
|
ENST00000698027.1:c.*661G>T
|
ENSP00000513505.1:n.*661G>T
|
|
ENST00000698028.1:n.2528G>T
|
|
|
ENST00000698029.1:n.3257G>T
|
|
|
ENST00000448276.7:c.*444G>T
MANE Select
|
ENSP00000392617.2:n.*444G>T
|
|
ENST00000448276.6:c.*444G>T
|
ENSP00000392617.2:n.*444G>T
|
|
ENST00000613943.4:c.1929G>T
|
ENSP00000483605.1:n.1929G>T
|
|
NM_001098426.1:c.*444G>T
|
NP_001091896.1:n.*444G>T
|
|
XM_005257604.2:c.*444G>T
|
XP_005257661.2:n.*444G>T
|
|
NM_001330439.1:c.*444G>T
|
NP_001317368.1:n.*444G>T
|
|
NM_001330440.1:c.*444G>T
|
NP_001317369.1:n.*444G>T
|
|
NM_001098426.2:c.*444G>T
MANE Select
|
NP_001091896.1:n.*444G>T
|
|
NM_001330440.2:c.*444G>T
|
NP_001317369.1:n.*444G>T
|
|