ENST00000366669.9:c.1910G>T
MANE Select
|
ENSP00000355629.4:p.Gly637Val
|
|
ENST00000366668.7:c.1907G>T
|
ENSP00000355628.3:p.Gly636Val
|
|
ENST00000366669.8:c.1910G>T
|
ENSP00000355629.4:p.Gly637Val
|
|
ENST00000468893.6:c.*1768G>T
|
ENSP00000476305.1:n.*1768G>T
|
|
ENST00000478710.1:n.169G>T
|
|
|
ENST00000490900.1:n.689G>T
|
|
|
ENST00000534989.1:c.1733G>T
|
ENSP00000440349.1:p.Gly578Val
|
|
NM_001145036.1:c.1907G>T
|
NP_001138508.1:p.Gly636Val
|
|
NM_007357.2:c.1910G>T
|
NP_031383.1:p.Gly637Val
|
|
NM_007357.3:c.1910G>T
MANE Select
|
NP_031383.1:p.Gly637Val
|
|
NM_001145036.2:c.1907G>T
|
NP_001138508.1:p.Gly636Val
|
|