ENST00000355832.10:c.1746G>T
MANE Select
|
ENSP00000348089.5:p.Val582=
|
|
ENST00000681632.1:n.1824G>T
|
|
|
ENST00000681659.1:c.1587G>T
|
ENSP00000505631.1:p.Val529=
|
|
ENST00000355832.9:c.1746G>T
|
ENSP00000348089.5:p.Val582=
|
|
ENST00000475116.1:n.275+7346G>T
|
|
|
ENST00000623073.3:c.147G>T
|
ENSP00000485650.1:p.Val49=
|
|
ENST00000623115.3:c.-70+7346G>T
|
ENSP00000485321.1:n.-70+7346G>T
|
|
ENST00000623318.1:c.147G>T
|
ENSP00000485423.1:p.Val49=
|
|
NM_000124.3:c.1746G>T
|
NP_000115.1:p.Val582=
|
|
NM_001346440.1:c.1746G>T
|
NP_001333369.1:p.Val582=
|
|
NM_000124.4:c.1746G>T
MANE Select
|
NP_000115.1:p.Val582=
|
|
NM_001346440.2:c.1746G>T
|
NP_001333369.1:p.Val582=
|
|