ENST00000355832.10:c.3907C>A
MANE Select
|
ENSP00000348089.5:p.Arg1303=
|
|
ENST00000679552.1:n.978C>A
|
|
|
ENST00000679871.1:n.1053C>A
|
|
|
ENST00000679974.1:n.956C>A
|
|
|
ENST00000681632.1:n.5310C>A
|
|
|
ENST00000681659.1:c.3748C>A
|
ENSP00000505631.1:p.Arg1250=
|
|
ENST00000355832.9:c.3907C>A
|
ENSP00000348089.5:p.Arg1303=
|
|
ENST00000465653.1:n.229C>A
|
|
|
ENST00000623073.3:c.*2203C>A
|
ENSP00000485650.1:n.*2203C>A
|
|
ENST00000623115.3:c.2017C>A
|
ENSP00000485321.1:p.Arg673=
|
|
ENST00000624341.3:c.1739C>A
|
|
|
NM_000124.3:c.3907C>A
|
NP_000115.1:p.Arg1303=
|
|
XR_945953.1:n.243-10137G>T
|
|
|
NM_001346440.1:c.3907C>A
|
NP_001333369.1:p.Arg1303=
|
|
NM_000124.4:c.3907C>A
MANE Select
|
NP_000115.1:p.Arg1303=
|
|
NM_001346440.2:c.3907C>A
|
NP_001333369.1:p.Arg1303=
|
|