ENST00000389857.11:c.3897C>T
MANE Select
|
ENSP00000374507.6:p.Arg1299=
|
|
ENST00000389857.10:c.3897C>T
|
ENSP00000374507.6:p.Arg1299=
|
|
NM_001080414.3:c.3897C>T
|
NP_001073883.2:p.Arg1299=
|
|
XM_005267691.3:c.3897C>T
|
XP_005267748.1:p.Arg1299=
|
|
XM_011536796.1:c.3789C>T
|
XP_011535098.1:p.Arg1263=
|
|
XR_429316.2:n.4025C>T
|
|
|
XR_943459.1:n.4025C>T
|
|
|
XM_005267691.5:c.3897C>T
|
XP_005267748.1:p.Arg1299=
|
|
XM_011536796.2:c.3789C>T
|
XP_011535098.1:p.Arg1263=
|
|
XM_017021335.2:c.3897C>T
|
XP_016876824.1:p.Arg1299=
|
|
XM_017021336.1:c.978C>T
|
XP_016876825.1:p.Arg326=
|
|
XR_429316.4:n.4023C>T
|
|
|
NM_001080414.4:c.3897C>T
MANE Select
|
NP_001073883.2:p.Arg1299=
|
|