ENST00000262027.10:c.1820C>A
MANE Select
|
ENSP00000262027.5:p.Ala607Asp
|
|
ENST00000262027.9:c.1820C>A
|
ENSP00000262027.5:p.Ala607Asp
|
|
ENST00000537638.6:c.*112C>A
|
ENSP00000446168.2:n.*112C>A
|
|
ENST00000545888.6:c.*1321C>A
|
ENSP00000439307.2:n.*1321C>A
|
|
ENST00000546971.5:n.564C>A
|
|
|
ENST00000548202.5:n.327C>A
|
|
|
ENST00000548944.1:c.134-3678C>A
|
ENSP00000449071.1:n.134-3678C>A
|
|
ENST00000549048.1:n.485C>A
|
|
|
ENST00000628866.2:c.*1321C>A
|
ENSP00000486738.1:n.*1321C>A
|
|
NM_004990.3:c.1820C>A
|
NP_004981.2:p.Ala607Asp
|
|
XM_006719398.2:c.1118C>A
|
XP_006719461.1:p.Ala373Asp
|
|
XM_011538353.1:c.*112C>A
|
XP_011536655.1:n.*112C>A
|
|
XM_006719398.4:c.1118C>A
|
XP_006719461.1:p.Ala373Asp
|
|
XR_001748704.2:n.1776C>A
|
|
|
XR_002957327.1:n.1767C>A
|
|
|
NM_004990.4:c.1820C>A
MANE Select
|
NP_004981.2:p.Ala607Asp
|
|