ENST00000366930.9:c.933-58G>C
MANE Select
|
ENSP00000355897.4:n.933-58G>C
|
|
ENST00000366929.4:c.1017-58G>C
|
ENSP00000355896.4:n.1017-58G>C
|
|
ENST00000366930.8:c.933-58G>C
|
ENSP00000355897.4:n.933-58G>C
|
|
ENST00000479322.1:n.417-58G>C
|
|
|
NM_001135599.2:c.1017-58G>C
|
NP_001129071.1:n.1017-58G>C
|
|
NM_003238.3:c.933-58G>C
|
NP_003229.1:n.933-58G>C
|
|
NM_001135599.3:c.1017-58G>C
|
NP_001129071.1:n.1017-58G>C
|
|
NM_003238.4:c.933-58G>C
|
NP_003229.1:n.933-58G>C
|
|
NR_138148.1:n.2236-58G>C
|
|
|
NR_138149.1:n.2320-58G>C
|
|
|
NM_003238.5:c.933-58G>C
|
NP_003229.1:n.933-58G>C
|
|
NM_003238.6:c.933-58G>C
MANE Select
|
NP_003229.1:n.933-58G>C
|
|
NM_001135599.4:c.1017-58G>C
|
NP_001129071.1:n.1017-58G>C
|
|
NR_138148.2:n.2184-58G>C
|
|
|
NR_138149.2:n.2268-58G>C
|
|
|