ENST00000355832.10:c.1533G>C
MANE Select
|
ENSP00000348089.5:p.Gln511His
|
|
ENST00000681632.1:n.1611G>C
|
|
|
ENST00000681659.1:c.1526+5194G>C
|
ENSP00000505631.1:n.1526+5194G>C
|
|
ENST00000355832.9:c.1533G>C
|
ENSP00000348089.5:p.Gln511His
|
|
ENST00000475116.1:n.123G>C
|
|
|
ENST00000623073.3:c.-67G>C
|
ENSP00000485650.1:n.-67G>C
|
|
ENST00000623115.3:c.-222G>C
|
ENSP00000485321.1:n.-222G>C
|
|
ENST00000623318.1:c.-67G>C
|
ENSP00000485423.1:n.-67G>C
|
|
ENST00000623788.1:n.532G>C
|
|
|
NM_000124.3:c.1533G>C
|
NP_000115.1:p.Gln511His
|
|
NM_001346440.1:c.1533G>C
|
NP_001333369.1:p.Gln511His
|
|
NM_000124.4:c.1533G>C
MANE Select
|
NP_000115.1:p.Gln511His
|
|
NM_001346440.2:c.1533G>C
|
NP_001333369.1:p.Gln511His
|
|