ENST00000355832.10:c.2965G>C
MANE Select
|
ENSP00000348089.5:p.Asp989His
|
|
ENST00000679552.1:n.142-191G>C
|
|
|
ENST00000679871.1:n.111G>C
|
|
|
ENST00000679974.1:n.120-191G>C
|
|
|
ENST00000681632.1:n.4368G>C
|
|
|
ENST00000681659.1:c.2806G>C
|
ENSP00000505631.1:p.Asp936His
|
|
ENST00000355832.9:c.2965G>C
|
ENSP00000348089.5:p.Asp989His
|
|
ENST00000623073.3:c.*1261G>C
|
ENSP00000485650.1:n.*1261G>C
|
|
ENST00000623115.3:c.1075G>C
|
ENSP00000485321.1:p.Asp359His
|
|
ENST00000624341.3:c.797G>C
|
|
|
NM_000124.3:c.2965G>C
|
NP_000115.1:p.Asp989His
|
|
XR_945953.1:n.243-485C>G
|
|
|
NM_001346440.1:c.2965G>C
|
NP_001333369.1:p.Asp989His
|
|
NM_000124.4:c.2965G>C
MANE Select
|
NP_000115.1:p.Asp989His
|
|
NM_001346440.2:c.2965G>C
|
NP_001333369.1:p.Asp989His
|
|