ENST00000697953.1:n.3276A>T
|
|
|
ENST00000698013.1:n.3388A>T
|
|
|
ENST00000698014.1:n.3611A>T
|
|
|
ENST00000698015.1:n.2704A>T
|
|
|
ENST00000698016.1:c.*828A>T
|
ENSP00000513502.1:n.*828A>T
|
|
ENST00000698017.1:n.2778A>T
|
|
|
ENST00000698018.1:n.2909A>T
|
|
|
ENST00000698019.1:n.3107A>T
|
|
|
ENST00000698020.1:n.2213A>T
|
|
|
ENST00000698021.1:c.2122A>T
|
|
|
ENST00000698022.1:c.*828A>T
|
ENSP00000513504.1:n.*828A>T
|
|
ENST00000698023.1:n.2807A>T
|
|
|
ENST00000698024.1:n.2669A>T
|
|
|
ENST00000448276.7:c.*828A>T
MANE Select
|
ENSP00000392617.2:n.*828A>T
|
|
ENST00000448276.6:c.*828A>T
|
ENSP00000392617.2:n.*828A>T
|
|
ENST00000613943.4:c.2313A>T
|
ENSP00000483605.1:n.2313A>T
|
|
NM_001098426.1:c.*828A>T
|
NP_001091896.1:n.*828A>T
|
|
XM_005257604.2:c.*828A>T
|
XP_005257661.2:n.*828A>T
|
|
NM_001330439.1:c.*828A>T
|
NP_001317368.1:n.*828A>T
|
|
NM_001330440.1:c.*828A>T
|
NP_001317369.1:n.*828A>T
|
|
NM_001098426.2:c.*828A>T
MANE Select
|
NP_001091896.1:n.*828A>T
|
|
NM_001330440.2:c.*828A>T
|
NP_001317369.1:n.*828A>T
|
|