ENST00000389857.11:c.979A>T
MANE Select
|
ENSP00000374507.6:p.Arg327Trp
|
|
ENST00000389857.10:c.979A>T
|
ENSP00000374507.6:p.Arg327Trp
|
|
ENST00000554051.1:n.456A>T
|
|
|
NM_001080414.3:c.979A>T
|
NP_001073883.2:p.Arg327Trp
|
|
XM_005267691.3:c.979A>T
|
XP_005267748.1:p.Arg327Trp
|
|
XM_011536796.1:c.871A>T
|
XP_011535098.1:p.Arg291Trp
|
|
XR_429316.2:n.1107A>T
|
|
|
XR_943459.1:n.1107A>T
|
|
|
XM_005267691.5:c.979A>T
|
XP_005267748.1:p.Arg327Trp
|
|
XM_011536796.2:c.871A>T
|
XP_011535098.1:p.Arg291Trp
|
|
XM_017021335.2:c.979A>T
|
XP_016876824.1:p.Arg327Trp
|
|
XM_017021337.2:c.979A>T
|
XP_016876826.1:p.Arg327Trp
|
|
XR_429316.4:n.1105A>T
|
|
|
NM_001080414.4:c.979A>T
MANE Select
|
NP_001073883.2:p.Arg327Trp
|
|