ENST00000355832.10:c.2002C>A
MANE Select
|
ENSP00000348089.5:p.Pro668Thr
|
|
ENST00000681632.1:n.2080C>A
|
|
|
ENST00000681659.1:c.1843C>A
|
ENSP00000505631.1:p.Pro615Thr
|
|
ENST00000355832.9:c.2002C>A
|
ENSP00000348089.5:p.Pro668Thr
|
|
ENST00000623073.3:c.*394C>A
|
ENSP00000485650.1:n.*394C>A
|
|
ENST00000623115.3:c.112C>A
|
ENSP00000485321.1:p.Pro38Thr
|
|
NM_000124.3:c.2002C>A
|
NP_000115.1:p.Pro668Thr
|
|
NM_001346440.1:c.2002C>A
|
NP_001333369.1:p.Pro668Thr
|
|
NM_000124.4:c.2002C>A
MANE Select
|
NP_000115.1:p.Pro668Thr
|
|
NM_001346440.2:c.2002C>A
|
NP_001333369.1:p.Pro668Thr
|
|