ENST00000615277.5:c.327+11788G>T
MANE Select
|
ENSP00000478458.1:n.327+11788G>T
|
|
ENST00000460467.1:n.438+94066G>T
|
|
|
ENST00000615277.4:c.327+11788G>T
|
ENSP00000478458.1:n.327+11788G>T
|
|
NM_001144382.1:c.327+11788G>T
|
NP_001137854.1:n.327+11788G>T
|
|
XM_006713073.3:c.-2519G>T
|
XP_006713136.1:n.-2519G>T
|
|
XM_017006022.2:c.327+11788G>T
|
XP_016861511.1:n.327+11788G>T
|
|
XM_017006023.1:c.327+11788G>T
|
XP_016861512.1:n.327+11788G>T
|
|
XM_017006024.2:c.327+11788G>T
|
XP_016861513.1:n.327+11788G>T
|
|
XM_017006025.1:c.-2686G>T
|
XP_016861514.1:n.-2686G>T
|
|
NM_001144382.2:c.327+11788G>T
MANE Select
|
NP_001137854.1:n.327+11788G>T
|
|