ENST00000355832.10:c.3112A>T
MANE Select
|
ENSP00000348089.5:p.Arg1038Ter
|
|
ENST00000679552.1:n.183A>T
|
|
|
ENST00000679871.1:n.258A>T
|
|
|
ENST00000679974.1:n.161A>T
|
|
|
ENST00000681632.1:n.4515A>T
|
|
|
ENST00000681659.1:c.2953A>T
|
ENSP00000505631.1:p.Arg985Ter
|
|
ENST00000355832.9:c.3112A>T
|
ENSP00000348089.5:p.Arg1038Ter
|
|
ENST00000623073.3:c.*1408A>T
|
ENSP00000485650.1:n.*1408A>T
|
|
ENST00000623115.3:c.1222A>T
|
ENSP00000485321.1:p.Arg408Ter
|
|
ENST00000624341.3:c.944A>T
|
|
|
NM_000124.3:c.3112A>T
|
NP_000115.1:p.Arg1038Ter
|
|
XR_945953.1:n.243-717T>A
|
|
|
NM_001346440.1:c.3112A>T
|
NP_001333369.1:p.Arg1038Ter
|
|
NM_000124.4:c.3112A>T
MANE Select
|
NP_000115.1:p.Arg1038Ter
|
|
NM_001346440.2:c.3112A>T
|
NP_001333369.1:p.Arg1038Ter
|
|