ENST00000710323.1:c.793+2T>C
|
ENSP00000518203.1:n.793+2T>C
|
|
ENST00000330877.7:c.793+2T>C
MANE Select
|
ENSP00000331260.2:n.793+2T>C
|
|
ENST00000330877.6:c.793+2T>C
|
ENSP00000331260.2:n.793+2T>C
|
|
ENST00000332972.9:c.922+2T>C
|
ENSP00000333019.5:n.922+2T>C
|
|
ENST00000553540.5:c.905+2T>C
|
ENSP00000450759.1:n.905+2T>C
|
|
ENST00000555486.5:c.858+2T>C
|
ENSP00000473778.1:n.858+2T>C
|
|
ENST00000557582.5:n.1714+2T>C
|
|
|
NM_152328.3:c.793+2T>C
|
NP_689541.1:n.793+2T>C
|
|
NM_199165.1:c.922+2T>C
|
NP_954634.1:n.922+2T>C
|
|
XM_006720026.2:c.796+2T>C
|
XP_006720089.1:n.796+2T>C
|
|
XM_011536412.1:c.925+2T>C
|
XP_011534714.1:n.925+2T>C
|
|
XM_011536413.1:c.610+2T>C
|
XP_011534715.1:n.610+2T>C
|
|
XM_011536414.1:c.607+2T>C
|
XP_011534716.1:n.607+2T>C
|
|
XM_011536415.1:c.178+2T>C
|
XP_011534717.1:n.178+2T>C
|
|
NM_001320424.1:c.178+2T>C
|
NP_001307353.1:n.178+2T>C
|
|
NM_152328.4:c.793+2T>C
|
NP_689541.1:n.793+2T>C
|
|
NM_199165.2:c.922+2T>C
|
NP_954634.1:n.922+2T>C
|
|
XM_006720026.3:c.796+2T>C
|
XP_006720089.1:n.796+2T>C
|
|
XM_011536412.2:c.925+2T>C
|
XP_011534714.1:n.925+2T>C
|
|
XR_001750917.1:n.464A>G
|
|
|
NM_152328.5:c.793+2T>C
MANE Select
|
NP_689541.1:n.793+2T>C
|
|