ENST00000262027.10:c.1814A>T
MANE Select
|
ENSP00000262027.5:p.Asp605Val
|
|
ENST00000262027.9:c.1814A>T
|
ENSP00000262027.5:p.Asp605Val
|
|
ENST00000537638.6:c.*106A>T
|
ENSP00000446168.2:n.*106A>T
|
|
ENST00000545888.6:c.*1315A>T
|
ENSP00000439307.2:n.*1315A>T
|
|
ENST00000546971.5:n.558A>T
|
|
|
ENST00000548202.5:n.321A>T
|
|
|
ENST00000548944.1:c.134-3684A>T
|
ENSP00000449071.1:n.134-3684A>T
|
|
ENST00000549048.1:n.479A>T
|
|
|
ENST00000628866.2:c.*1315A>T
|
ENSP00000486738.1:n.*1315A>T
|
|
NM_004990.3:c.1814A>T
|
NP_004981.2:p.Asp605Val
|
|
XM_006719398.2:c.1112A>T
|
XP_006719461.1:p.Asp371Val
|
|
XM_011538353.1:c.*106A>T
|
XP_011536655.1:n.*106A>T
|
|
XM_006719398.4:c.1112A>T
|
XP_006719461.1:p.Asp371Val
|
|
XR_001748704.2:n.1770A>T
|
|
|
XR_002957327.1:n.1761A>T
|
|
|
NM_004990.4:c.1814A>T
MANE Select
|
NP_004981.2:p.Asp605Val
|
|