|
NM_001002295.2:c.*266dup
MANE Select
|
NP_001002295.1:n.*266dup
|
|
ENST00000379328.9:c.*266dup
MANE Select
|
ENSP00000368632.3:n.*266dup
|
|
NM_001002295.1:c.*266dup
|
NP_001002295.1:n.*266dup
|
|
NM_002051.2:c.*266dup
|
NP_002042.1:n.*266dup
|
|
NM_002051.3:c.*266dup
|
NP_002042.1:n.*266dup
|
|
ENST00000346208.3:c.*266dup
|
ENSP00000341619.3:n.*266dup
|
|
ENST00000346208.4:c.*266dup
|
ENSP00000341619.3:n.*266dup
|
|
ENST00000379328.7:c.*266dup
|
ENSP00000368632.3:n.*266dup
|
|
XM_005252442.2:c.*266dup
|
XP_005252499.1:n.*266dup
|
|
XM_005252443.3:c.*266dup
|
XP_005252500.1:n.*266dup
|
|
XM_005252443.5:c.*266dup
|
XP_005252500.1:n.*266dup
|