ENST00000515059.6:c.-113+59522T>C
MANE Select
|
ENSP00000426617.1:n.-113+59522T>C
|
|
ENST00000515059.5:c.-113+59522T>C
|
ENSP00000426617.1:n.-113+59522T>C
|
|
NM_001203.2:c.-113+59522T>C
|
NP_001194.1:n.-113+59522T>C
|
|
XM_011532201.1:c.-18+59522T>C
|
XP_011530503.1:n.-18+59522T>C
|
|
XM_011532201.2:c.-18+59522T>C
|
XP_011530503.1:n.-18+59522T>C
|
|
XM_017008558.1:c.-113+59522T>C
|
XP_016864047.1:n.-113+59522T>C
|
|
XM_017008559.1:c.-113+36372T>C
|
XP_016864048.1:n.-113+36372T>C
|
|
NM_001203.3:c.-113+59522T>C
MANE Select
|
NP_001194.1:n.-113+59522T>C
|
|