ENST00000374479.4:c.390-272T>C
MANE Select
|
ENSP00000363603.3:n.390-272T>C
|
|
ENST00000374479.3:c.390-272T>C
|
ENSP00000363603.3:n.390-272T>C
|
|
NM_000147.4:c.390-272T>C
|
NP_000138.2:n.390-272T>C
|
|
XM_005245821.1:c.15-272T>C
|
XP_005245878.1:n.15-272T>C
|
|
XM_011541167.1:c.-245+13T>C
|
XP_011539469.1:n.-245+13T>C
|
|
XM_005245821.3:c.15-272T>C
|
XP_005245878.1:n.15-272T>C
|
|
XM_011541167.3:c.-245+13T>C
|
XP_011539469.1:n.-245+13T>C
|
|
XM_017000905.2:c.87-272T>C
|
XP_016856394.1:n.87-272T>C
|
|
NM_000147.5:c.390-272T>C
MANE Select
|
NP_000138.2:n.390-272T>C
|
|
NR_174379.1:n.568-272T>C
|
|
|
NR_174380.1:n.617-272T>C
|
|
|
NR_174381.1:n.455+13T>C
|
|
|
NR_174382.1:n.852+13T>C
|
|
|