ENST00000697953.1:n.3295T>C
|
|
|
ENST00000698013.1:n.3407T>C
|
|
|
ENST00000698014.1:n.3630T>C
|
|
|
ENST00000698015.1:n.2723T>C
|
|
|
ENST00000698016.1:c.*847T>C
|
ENSP00000513502.1:n.*847T>C
|
|
ENST00000448276.7:c.*847T>C
MANE Select
|
ENSP00000392617.2:n.*847T>C
|
|
ENST00000448276.6:c.*847T>C
|
ENSP00000392617.2:n.*847T>C
|
|
ENST00000613943.4:c.2332T>C
|
ENSP00000483605.1:n.2332T>C
|
|
NM_001098426.1:c.*847T>C
|
NP_001091896.1:n.*847T>C
|
|
XM_005257604.2:c.*847T>C
|
XP_005257661.2:n.*847T>C
|
|
NM_001330439.1:c.*847T>C
|
NP_001317368.1:n.*847T>C
|
|
NM_001330440.1:c.*847T>C
|
NP_001317369.1:n.*847T>C
|
|
NM_001098426.2:c.*847T>C
MANE Select
|
NP_001091896.1:n.*847T>C
|
|
NM_001330440.2:c.*847T>C
|
NP_001317369.1:n.*847T>C
|
|