ENST00000367466.4:c.-70+10176G>C
MANE Select
|
ENSP00000356436.3:n.-70+10176G>C
|
|
ENST00000367466.3:c.-70+10176G>C
|
ENSP00000356436.3:n.-70+10176G>C
|
|
NM_001311193.1:c.-70+10176G>C
|
NP_001298122.1:n.-70+10176G>C
|
|
NM_024420.2:c.-70+10176G>C
|
NP_077734.1:n.-70+10176G>C
|
|
XM_011509642.1:c.-70+10161G>C
|
XP_011507944.1:n.-70+10161G>C
|
|
XM_011509642.2:c.-70+10161G>C
|
XP_011507944.1:n.-70+10161G>C
|
|
NM_001311193.2:c.-70+10176G>C
|
NP_001298122.2:n.-70+10176G>C
|
|
NM_024420.3:c.-70+10176G>C
MANE Select
|
NP_077734.2:n.-70+10176G>C
|
|