ENST00000355832.10:c.2097G>A
MANE Select
|
ENSP00000348089.5:p.Thr699=
|
|
ENST00000681632.1:n.2175G>A
|
|
|
ENST00000681659.1:c.1938G>A
|
ENSP00000505631.1:p.Thr646=
|
|
ENST00000355832.9:c.2097G>A
|
ENSP00000348089.5:p.Thr699=
|
|
ENST00000623073.3:c.*489G>A
|
ENSP00000485650.1:n.*489G>A
|
|
ENST00000623115.3:c.207G>A
|
ENSP00000485321.1:p.Thr69=
|
|
NM_000124.3:c.2097G>A
|
NP_000115.1:p.Thr699=
|
|
NM_001346440.1:c.2097G>A
|
NP_001333369.1:p.Thr699=
|
|
NM_000124.4:c.2097G>A
MANE Select
|
NP_000115.1:p.Thr699=
|
|
NM_001346440.2:c.2097G>A
|
NP_001333369.1:p.Thr699=
|
|