ENST00000366669.9:c.1854T>G
MANE Select
|
ENSP00000355629.4:p.Leu618=
|
|
ENST00000366668.7:c.1851T>G
|
ENSP00000355628.3:p.Leu617=
|
|
ENST00000366669.8:c.1854T>G
|
ENSP00000355629.4:p.Leu618=
|
|
ENST00000468893.6:c.*1712T>G
|
ENSP00000476305.1:n.*1712T>G
|
|
ENST00000478710.1:n.113T>G
|
|
|
ENST00000490900.1:n.633T>G
|
|
|
ENST00000534989.1:c.1677T>G
|
ENSP00000440349.1:p.Leu559=
|
|
NM_001145036.1:c.1851T>G
|
NP_001138508.1:p.Leu617=
|
|
NM_007357.2:c.1854T>G
|
NP_031383.1:p.Leu618=
|
|
NM_007357.3:c.1854T>G
MANE Select
|
NP_031383.1:p.Leu618=
|
|
NM_001145036.2:c.1851T>G
|
NP_001138508.1:p.Leu617=
|
|