ENST00000355832.10:c.2945T>A
MANE Select
|
ENSP00000348089.5:p.Leu982Ter
|
|
ENST00000679552.1:n.142-211T>A
|
|
|
ENST00000679871.1:n.91T>A
|
|
|
ENST00000679974.1:n.120-211T>A
|
|
|
ENST00000681632.1:n.4348T>A
|
|
|
ENST00000681659.1:c.2786T>A
|
ENSP00000505631.1:p.Leu929Ter
|
|
ENST00000355832.9:c.2945T>A
|
ENSP00000348089.5:p.Leu982Ter
|
|
ENST00000623073.3:c.*1241T>A
|
ENSP00000485650.1:n.*1241T>A
|
|
ENST00000623115.3:c.1055T>A
|
ENSP00000485321.1:p.Leu352Ter
|
|
ENST00000624341.3:c.777T>A
|
|
|
NM_000124.3:c.2945T>A
|
NP_000115.1:p.Leu982Ter
|
|
XR_945953.1:n.243-465A>T
|
|
|
NM_001346440.1:c.2945T>A
|
NP_001333369.1:p.Leu982Ter
|
|
NM_000124.4:c.2945T>A
MANE Select
|
NP_000115.1:p.Leu982Ter
|
|
NM_001346440.2:c.2945T>A
|
NP_001333369.1:p.Leu982Ter
|
|