ENST00000584483.6:n.2613G>T
|
|
|
ENST00000697953.1:n.3186G>T
|
|
|
ENST00000698013.1:n.3298G>T
|
|
|
ENST00000698014.1:n.3521G>T
|
|
|
ENST00000698015.1:n.2614G>T
|
|
|
ENST00000698016.1:c.*738G>T
|
ENSP00000513502.1:n.*738G>T
|
|
ENST00000698017.1:n.2688G>T
|
|
|
ENST00000698018.1:n.2819G>T
|
|
|
ENST00000698019.1:n.3017G>T
|
|
|
ENST00000698020.1:n.2123G>T
|
|
|
ENST00000698021.1:c.2032G>T
|
|
|
ENST00000698022.1:c.*738G>T
|
ENSP00000513504.1:n.*738G>T
|
|
ENST00000698023.1:n.2717G>T
|
|
|
ENST00000698024.1:n.2579G>T
|
|
|
ENST00000698025.1:n.2739G>T
|
|
|
ENST00000698026.1:n.1630G>T
|
|
|
ENST00000698027.1:c.*955G>T
|
ENSP00000513505.1:n.*955G>T
|
|
ENST00000698028.1:n.2822G>T
|
|
|
ENST00000448276.7:c.*738G>T
MANE Select
|
ENSP00000392617.2:n.*738G>T
|
|
ENST00000448276.6:c.*738G>T
|
ENSP00000392617.2:n.*738G>T
|
|
ENST00000613943.4:c.2223G>T
|
ENSP00000483605.1:n.2223G>T
|
|
NM_001098426.1:c.*738G>T
|
NP_001091896.1:n.*738G>T
|
|
XM_005257604.2:c.*738G>T
|
XP_005257661.2:n.*738G>T
|
|
NM_001330439.1:c.*738G>T
|
NP_001317368.1:n.*738G>T
|
|
NM_001330440.1:c.*738G>T
|
NP_001317369.1:n.*738G>T
|
|
NM_001098426.2:c.*738G>T
MANE Select
|
NP_001091896.1:n.*738G>T
|
|
NM_001330440.2:c.*738G>T
|
NP_001317369.1:n.*738G>T
|
|