ENST00000355832.10:c.3587T>G
MANE Select
|
ENSP00000348089.5:p.Leu1196Arg
|
|
ENST00000679552.1:n.658T>G
|
|
|
ENST00000679871.1:n.733T>G
|
|
|
ENST00000679974.1:n.636T>G
|
|
|
ENST00000681632.1:n.4990T>G
|
|
|
ENST00000681659.1:c.3428T>G
|
ENSP00000505631.1:p.Leu1143Arg
|
|
ENST00000355832.9:c.3587T>G
|
ENSP00000348089.5:p.Leu1196Arg
|
|
ENST00000623073.3:c.*1883T>G
|
ENSP00000485650.1:n.*1883T>G
|
|
ENST00000623115.3:c.1697T>G
|
ENSP00000485321.1:p.Leu566Arg
|
|
ENST00000624341.3:c.1419T>G
|
|
|
NM_000124.3:c.3587T>G
|
NP_000115.1:p.Leu1196Arg
|
|
XR_945953.1:n.243-1192A>C
|
|
|
NM_001346440.1:c.3587T>G
|
NP_001333369.1:p.Leu1196Arg
|
|
NM_000124.4:c.3587T>G
MANE Select
|
NP_000115.1:p.Leu1196Arg
|
|
NM_001346440.2:c.3587T>G
|
NP_001333369.1:p.Leu1196Arg
|
|