ENST00000302850.10:c.4027C>T
MANE Select
|
ENSP00000303830.4:p.Arg1343Trp
|
|
ENST00000302850.9:c.4027C>T
|
ENSP00000303830.4:p.Arg1343Trp
|
|
ENST00000341500.9:c.3991C>T
|
ENSP00000342838.4:p.Arg1331Trp
|
|
NM_000208.2:c.4027C>T
|
NP_000199.2:p.Arg1343Trp
|
|
NM_000208.3:c.4027C>T
|
NP_000199.2:p.Arg1343Trp
|
|
NM_001079817.1:c.3991C>T
|
NP_001073285.1:p.Arg1331Trp
|
|
NM_001079817.2:c.3991C>T
|
NP_001073285.1:p.Arg1331Trp
|
|
XM_011527988.1:c.4102C>T
|
XP_011526290.1:p.Arg1368Trp
|
|
XM_011527989.1:c.4066C>T
|
XP_011526291.1:p.Arg1356Trp
|
|
XM_011527988.2:c.4024C>T
|
XP_011526290.2:p.Arg1342Trp
|
|
XM_011527989.3:c.3988C>T
|
XP_011526291.2:p.Arg1330Trp
|
|
NM_000208.4:c.4027C>T
MANE Select
|
NP_000199.2:p.Arg1343Trp
|
|
NM_001079817.3:c.3991C>T
|
NP_001073285.1:p.Arg1331Trp
|
|