ENST00000584483.6:n.2586G>A
|
|
|
ENST00000697953.1:n.3159G>A
|
|
|
ENST00000698013.1:n.3271G>A
|
|
|
ENST00000698014.1:n.3494G>A
|
|
|
ENST00000698015.1:n.2587G>A
|
|
|
ENST00000698016.1:c.*711G>A
|
ENSP00000513502.1:n.*711G>A
|
|
ENST00000698017.1:n.2661G>A
|
|
|
ENST00000698018.1:n.2792G>A
|
|
|
ENST00000698019.1:n.2990G>A
|
|
|
ENST00000698020.1:n.2096G>A
|
|
|
ENST00000698021.1:c.2005G>A
|
|
|
ENST00000698022.1:c.*711G>A
|
ENSP00000513504.1:n.*711G>A
|
|
ENST00000698023.1:n.2690G>A
|
|
|
ENST00000698024.1:n.2552G>A
|
|
|
ENST00000698025.1:n.2712G>A
|
|
|
ENST00000698026.1:n.1603G>A
|
|
|
ENST00000698027.1:c.*928G>A
|
ENSP00000513505.1:n.*928G>A
|
|
ENST00000698028.1:n.2795G>A
|
|
|
ENST00000448276.7:c.*711G>A
MANE Select
|
ENSP00000392617.2:n.*711G>A
|
|
ENST00000448276.6:c.*711G>A
|
ENSP00000392617.2:n.*711G>A
|
|
ENST00000613943.4:c.2196G>A
|
ENSP00000483605.1:n.2196G>A
|
|
NM_001098426.1:c.*711G>A
|
NP_001091896.1:n.*711G>A
|
|
XM_005257604.2:c.*711G>A
|
XP_005257661.2:n.*711G>A
|
|
NM_001330439.1:c.*711G>A
|
NP_001317368.1:n.*711G>A
|
|
NM_001330440.1:c.*711G>A
|
NP_001317369.1:n.*711G>A
|
|
NM_001098426.2:c.*711G>A
MANE Select
|
NP_001091896.1:n.*711G>A
|
|
NM_001330440.2:c.*711G>A
|
NP_001317369.1:n.*711G>A
|
|