ENST00000355832.10:c.3126A>T
MANE Select
|
ENSP00000348089.5:p.Pro1042=
|
|
ENST00000679552.1:n.197A>T
|
|
|
ENST00000679871.1:n.272A>T
|
|
|
ENST00000679974.1:n.175A>T
|
|
|
ENST00000681632.1:n.4529A>T
|
|
|
ENST00000681659.1:c.2967A>T
|
ENSP00000505631.1:p.Pro989=
|
|
ENST00000355832.9:c.3126A>T
|
ENSP00000348089.5:p.Pro1042=
|
|
ENST00000623073.3:c.*1422A>T
|
ENSP00000485650.1:n.*1422A>T
|
|
ENST00000623115.3:c.1236A>T
|
ENSP00000485321.1:p.Pro412=
|
|
ENST00000624341.3:c.958A>T
|
|
|
NM_000124.3:c.3126A>T
|
NP_000115.1:p.Pro1042=
|
|
XR_945953.1:n.243-731T>A
|
|
|
NM_001346440.1:c.3126A>T
|
NP_001333369.1:p.Pro1042=
|
|
NM_000124.4:c.3126A>T
MANE Select
|
NP_000115.1:p.Pro1042=
|
|
NM_001346440.2:c.3126A>T
|
NP_001333369.1:p.Pro1042=
|
|