ENST00000355832.10:c.1719T>C
MANE Select
|
ENSP00000348089.5:p.Cys573=
|
|
ENST00000681632.1:n.1797T>C
|
|
|
ENST00000681659.1:c.1560T>C
|
ENSP00000505631.1:p.Cys520=
|
|
ENST00000355832.9:c.1719T>C
|
ENSP00000348089.5:p.Cys573=
|
|
ENST00000475116.1:n.275+7319T>C
|
|
|
ENST00000623073.3:c.120T>C
|
ENSP00000485650.1:p.Cys40=
|
|
ENST00000623115.3:c.-70+7319T>C
|
ENSP00000485321.1:n.-70+7319T>C
|
|
ENST00000623318.1:c.120T>C
|
ENSP00000485423.1:p.Cys40=
|
|
NM_000124.3:c.1719T>C
|
NP_000115.1:p.Cys573=
|
|
NM_001346440.1:c.1719T>C
|
NP_001333369.1:p.Cys573=
|
|
NM_000124.4:c.1719T>C
MANE Select
|
NP_000115.1:p.Cys573=
|
|
NM_001346440.2:c.1719T>C
|
NP_001333369.1:p.Cys573=
|
|