ENST00000263440.6:c.921G>C
MANE Select
|
ENSP00000263440.5:p.Leu307Phe
|
|
ENST00000603108.6:c.*70G>C
|
ENSP00000473934.2:n.*70G>C
|
|
ENST00000647818.1:c.*227G>C
|
ENSP00000497667.1:n.*227G>C
|
|
ENST00000648964.1:c.*650G>C
|
ENSP00000497828.1:n.*650G>C
|
|
ENST00000649570.1:c.*343G>C
|
ENSP00000497742.1:n.*343G>C
|
|
ENST00000650494.1:c.*278G>C
|
ENSP00000497170.1:n.*278G>C
|
|
ENST00000263440.4:c.927G>C
|
ENSP00000263440.4:p.Leu309Phe
|
|
ENST00000371108.8:c.921G>C
|
ENSP00000360149.4:p.Leu307Phe
|
|
ENST00000465969.5:n.510G>C
|
|
|
ENST00000603108.5:c.845G>C
|
ENSP00000473934.1:p.Ter282Ser
|
|
NM_013339.3:c.921G>C
|
NP_037471.2:p.Leu307Phe
|
|
NM_013339.4:c.921G>C
MANE Select
|
NP_037471.2:p.Leu307Phe
|
|