ENST00000370397.8:c.933+1215T>C
MANE Select
|
ENSP00000359424.6:n.933+1215T>C
|
|
ENST00000370397.7:c.933+1215T>C
|
ENSP00000359424.6:n.933+1215T>C
|
|
NM_001278.3:c.933+1215T>C
|
NP_001269.3:n.933+1215T>C
|
|
XM_011539196.1:c.933+1215T>C
|
XP_011537498.1:n.933+1215T>C
|
|
XM_011539197.1:c.933+1215T>C
|
XP_011537499.1:n.933+1215T>C
|
|
XM_011539198.1:c.933+1215T>C
|
XP_011537500.1:n.933+1215T>C
|
|
XR_945589.1:n.1011+1215T>C
|
|
|
XR_945590.1:n.1011+1215T>C
|
|
|
NM_001278.4:c.933+1215T>C
|
NP_001269.3:n.933+1215T>C
|
|
NM_001320928.1:c.933+1215T>C
|
NP_001307857.1:n.933+1215T>C
|
|
XM_017015611.1:c.933+1215T>C
|
XP_016871100.1:n.933+1215T>C
|
|
XM_017015612.1:c.933+1215T>C
|
XP_016871101.1:n.933+1215T>C
|
|
XR_001747010.1:n.1011+1215T>C
|
|
|
XR_001747011.1:n.1011+1215T>C
|
|
|
NM_001278.5:c.933+1215T>C
MANE Select
|
NP_001269.3:n.933+1215T>C
|
|
NM_001320928.2:c.933+1215T>C
|
NP_001307857.1:n.933+1215T>C
|
|