ENST00000263038.9:c.603G>T
MANE Select
|
ENSP00000263038.4:p.Arg201=
|
|
ENST00000263038.8:c.603G>T
|
ENSP00000263038.4:p.Arg201=
|
|
ENST00000396913.6:c.303G>T
|
ENSP00000380121.2:p.Arg101=
|
|
ENST00000396920.7:c.552G>T
|
ENSP00000380126.3:p.Arg184=
|
|
ENST00000453759.6:c.303G>T
|
ENSP00000412525.2:p.Arg101=
|
|
ENST00000479604.1:c.609G>T
|
ENSP00000420117.1:p.Arg203=
|
|
NM_001037537.1:c.303G>T
|
NP_001032626.1:p.Arg101=
|
|
NM_006214.3:c.603G>T
|
NP_006205.1:p.Arg201=
|
|
XM_005252469.2:c.460-4596G>T
|
XP_005252526.1:n.460-4596G>T
|
|
NM_001323080.1:c.303G>T
|
NP_001310009.1:p.Arg101=
|
|
NM_001323082.1:c.609G>T
|
NP_001310011.1:p.Arg203=
|
|
NM_001323083.1:c.415-4596G>T
|
NP_001310012.1:n.415-4596G>T
|
|
NM_001323084.1:c.309G>T
|
NP_001310013.1:p.Arg103=
|
|
NM_006214.4:c.603G>T
MANE Select
|
NP_006205.1:p.Arg201=
|
|
NM_001037537.2:c.303G>T
|
NP_001032626.1:p.Arg101=
|
|
NM_001323080.2:c.303G>T
|
NP_001310009.1:p.Arg101=
|
|
NM_001323082.2:c.609G>T
|
NP_001310011.1:p.Arg203=
|
|
NM_001323083.2:c.415-4596G>T
|
NP_001310012.1:n.415-4596G>T
|
|
NM_001323084.2:c.309G>T
|
NP_001310013.1:p.Arg103=
|
|