|
NM_019101.3:c.294G>T
(APOM)
MANE Select
|
NP_061974.2:p.Arg98=
|
|
ENST00000375916.4:c.294G>T
(APOM)
MANE Select
|
ENSP00000365081.3:p.Arg98=
|
|
NM_001256169.1:c.78G>T
(APOM)
|
NP_001243098.1:p.Arg26=
|
|
NM_001256169.2:c.78G>T
(APOM)
|
NP_001243098.1:p.Arg26=
|
|
NM_019101.2:c.294G>T
(APOM)
|
NP_061974.2:p.Arg98=
|
|
NR_045828.1:n.329G>T
(APOM)
|
|
|
NR_045828.2:n.335G>T
(APOM)
|
|
|
ENST00000375916.3:c.294G>T
(APOM)
|
ENSP00000365081.3:p.Arg98=
|
|
ENST00000375918.6:c.78G>T
(APOM)
|
ENSP00000365083.2:p.Arg26=
|
|
ENST00000375920.8:c.78G>T
(APOM)
|
ENSP00000365085.4:p.Arg26=
|
|
XM_006715150.2:c.198G>T
(APOM)
|
XP_006715213.1:p.Arg66=
|
|
XM_006715150.3:c.198G>T
(APOM)
|
XP_006715213.1:p.Arg66=
|
|
XM_011514895.1:c.-14+3072C>A
(BAG6)
|
XP_011513197.1:n.-14+3072C>A
|
|
XM_017011279.2:c.-14+3072C>A
(BAG6)
|
XP_016866768.1:n.-14+3072C>A
|
|
XM_024446545.1:c.-14+515C>A
(BAG6)
|
XP_024302313.1:n.-14+515C>A
|
