ENST00000584483.6:n.2632G>A
|
|
|
ENST00000697953.1:n.3205G>A
|
|
|
ENST00000698013.1:n.3317G>A
|
|
|
ENST00000698014.1:n.3540G>A
|
|
|
ENST00000698015.1:n.2633G>A
|
|
|
ENST00000698016.1:c.*757G>A
|
ENSP00000513502.1:n.*757G>A
|
|
ENST00000698017.1:n.2707G>A
|
|
|
ENST00000698018.1:n.2838G>A
|
|
|
ENST00000698019.1:n.3036G>A
|
|
|
ENST00000698020.1:n.2142G>A
|
|
|
ENST00000698021.1:c.2051G>A
|
|
|
ENST00000698022.1:c.*757G>A
|
ENSP00000513504.1:n.*757G>A
|
|
ENST00000698023.1:n.2736G>A
|
|
|
ENST00000698024.1:n.2598G>A
|
|
|
ENST00000698025.1:n.2758G>A
|
|
|
ENST00000698026.1:n.1649G>A
|
|
|
ENST00000698027.1:c.*974G>A
|
ENSP00000513505.1:n.*974G>A
|
|
ENST00000448276.7:c.*757G>A
MANE Select
|
ENSP00000392617.2:n.*757G>A
|
|
ENST00000448276.6:c.*757G>A
|
ENSP00000392617.2:n.*757G>A
|
|
ENST00000613943.4:c.2242G>A
|
ENSP00000483605.1:n.2242G>A
|
|
NM_001098426.1:c.*757G>A
|
NP_001091896.1:n.*757G>A
|
|
XM_005257604.2:c.*757G>A
|
XP_005257661.2:n.*757G>A
|
|
NM_001330439.1:c.*757G>A
|
NP_001317368.1:n.*757G>A
|
|
NM_001330440.1:c.*757G>A
|
NP_001317369.1:n.*757G>A
|
|
NM_001098426.2:c.*757G>A
MANE Select
|
NP_001091896.1:n.*757G>A
|
|
NM_001330440.2:c.*757G>A
|
NP_001317369.1:n.*757G>A
|
|