ENST00000346342.8:c.364+133T>C
MANE Select
|
ENSP00000329546.4:n.364+133T>C
|
|
ENST00000346342.7:c.364+133T>C
|
ENSP00000329546.3:n.364+133T>C
|
|
ENST00000375581.3:c.430+133T>C
|
ENSP00000364731.3:n.430+133T>C
|
|
ENST00000444337.1:c.*172+133T>C
|
ENSP00000387669.1:n.*172+133T>C
|
|
ENST00000473085.1:n.311+133T>C
|
|
|
ENST00000479674.1:n.697+133T>C
|
|
|
ENST00000541084.5:c.178+133T>C
|
ENSP00000442051.2:n.178+133T>C
|
|
NM_000131.4:c.430+133T>C , LRG_554t1:c.430+133T>C
|
NP_000122.1:n.430+133T>C
|
|
NM_001267554.1:c.178+133T>C
|
NP_001254483.1:n.178+133T>C
|
|
NM_019616.3:c.364+133T>C , LRG_554t2:c.364+133T>C
|
NP_062562.1:n.364+133T>C
|
|
NR_051961.1:n.451+133T>C
|
|
|
XM_006719963.2:c.364+133T>C
|
XP_006720026.1:n.364+133T>C
|
|
XM_011537474.1:c.364+133T>C
|
XP_011535776.1:n.364+133T>C
|
|
XM_011537475.1:c.178+133T>C
|
XP_011535777.1:n.178+133T>C
|
|
XM_011537477.1:c.325+133T>C
|
XP_011535779.1:n.325+133T>C
|
|
XM_006719963.3:c.409+133T>C
|
XP_006720026.2:n.409+133T>C
|
|
XM_011537474.2:c.409+133T>C
|
XP_011535776.2:n.409+133T>C
|
|
XM_011537475.2:c.223+133T>C
|
XP_011535777.2:n.223+133T>C
|
|
XM_011537476.2:c.-676T>C
|
XP_011535778.1:n.-676T>C
|
|
NM_019616.4:c.364+133T>C
MANE Select
|
NP_062562.1:n.364+133T>C
|
|
NR_051961.2:n.448+133T>C
|
|
|
NM_001267554.2:c.178+133T>C
|
NP_001254483.1:n.178+133T>C
|
|