ENST00000355832.10:c.3953G>T
MANE Select
|
ENSP00000348089.5:p.Arg1318Met
|
|
ENST00000679552.1:n.1024G>T
|
|
|
ENST00000679871.1:n.1099G>T
|
|
|
ENST00000679974.1:n.1002G>T
|
|
|
ENST00000681632.1:n.5356G>T
|
|
|
ENST00000681659.1:c.3794G>T
|
ENSP00000505631.1:p.Arg1265Met
|
|
ENST00000355832.9:c.3953G>T
|
ENSP00000348089.5:p.Arg1318Met
|
|
ENST00000465653.1:n.275G>T
|
|
|
ENST00000623073.3:c.*2249G>T
|
ENSP00000485650.1:n.*2249G>T
|
|
ENST00000623115.3:c.2063G>T
|
ENSP00000485321.1:p.Arg688Met
|
|
ENST00000624341.3:c.1785G>T
|
|
|
NM_000124.3:c.3953G>T
|
NP_000115.1:p.Arg1318Met
|
|
XR_945953.1:n.243-10183C>A
|
|
|
NM_001346440.1:c.3953G>T
|
NP_001333369.1:p.Arg1318Met
|
|
NM_000124.4:c.3953G>T
MANE Select
|
NP_000115.1:p.Arg1318Met
|
|
NM_001346440.2:c.3953G>T
|
NP_001333369.1:p.Arg1318Met
|
|