ENST00000366930.9:c.643+40T>C
MANE Select
|
ENSP00000355897.4:n.643+40T>C
|
|
ENST00000366929.4:c.727+40T>C
|
ENSP00000355896.4:n.727+40T>C
|
|
ENST00000366930.8:c.643+40T>C
|
ENSP00000355897.4:n.643+40T>C
|
|
ENST00000479322.1:n.127+2T>C
|
|
|
ENST00000488793.1:n.347T>C
|
|
|
NM_001135599.2:c.727+40T>C
|
NP_001129071.1:n.727+40T>C
|
|
NM_003238.3:c.643+40T>C
|
NP_003229.1:n.643+40T>C
|
|
NM_001135599.3:c.727+40T>C
|
NP_001129071.1:n.727+40T>C
|
|
NM_003238.4:c.643+40T>C
|
NP_003229.1:n.643+40T>C
|
|
NR_138148.1:n.2061+40T>C
|
|
|
NR_138149.1:n.2145+40T>C
|
|
|
NM_003238.5:c.643+40T>C
|
NP_003229.1:n.643+40T>C
|
|
NM_003238.6:c.643+40T>C
MANE Select
|
NP_003229.1:n.643+40T>C
|
|
NM_001135599.4:c.727+40T>C
|
NP_001129071.1:n.727+40T>C
|
|
NR_138148.2:n.2009+40T>C
|
|
|
NR_138149.2:n.2093+40T>C
|
|
|