ENST00000366669.9:c.1842C>T
MANE Select
|
ENSP00000355629.4:p.Pro614=
|
|
ENST00000366668.7:c.1839C>T
|
ENSP00000355628.3:p.Pro613=
|
|
ENST00000366669.8:c.1842C>T
|
ENSP00000355629.4:p.Pro614=
|
|
ENST00000468893.6:c.*1700C>T
|
ENSP00000476305.1:n.*1700C>T
|
|
ENST00000478710.1:n.101C>T
|
|
|
ENST00000490900.1:n.621C>T
|
|
|
ENST00000534989.1:c.1665C>T
|
ENSP00000440349.1:p.Pro555=
|
|
NM_001145036.1:c.1839C>T
|
NP_001138508.1:p.Pro613=
|
|
NM_007357.2:c.1842C>T
|
NP_031383.1:p.Pro614=
|
|
NM_007357.3:c.1842C>T
MANE Select
|
NP_031383.1:p.Pro614=
|
|
NM_001145036.2:c.1839C>T
|
NP_001138508.1:p.Pro613=
|
|