ENST00000355832.10:c.3158G>A
MANE Select
|
ENSP00000348089.5:p.Arg1053His
|
|
ENST00000679552.1:n.229G>A
|
|
|
ENST00000679871.1:n.304G>A
|
|
|
ENST00000679974.1:n.207G>A
|
|
|
ENST00000681632.1:n.4561G>A
|
|
|
ENST00000681659.1:c.2999G>A
|
ENSP00000505631.1:p.Arg1000His
|
|
ENST00000355832.9:c.3158G>A
|
ENSP00000348089.5:p.Arg1053His
|
|
ENST00000623073.3:c.*1454G>A
|
ENSP00000485650.1:n.*1454G>A
|
|
ENST00000623115.3:c.1268G>A
|
ENSP00000485321.1:p.Arg423His
|
|
ENST00000624341.3:c.990G>A
|
|
|
NM_000124.3:c.3158G>A
|
NP_000115.1:p.Arg1053His
|
|
XR_945953.1:n.243-763C>T
|
|
|
NM_001346440.1:c.3158G>A
|
NP_001333369.1:p.Arg1053His
|
|
NM_000124.4:c.3158G>A
MANE Select
|
NP_000115.1:p.Arg1053His
|
|
NM_001346440.2:c.3158G>A
|
NP_001333369.1:p.Arg1053His
|
|