|
ENST00000375916.4:c.269+254C>T
(APOM)
MANE Select
|
ENSP00000365081.3:n.269+254C>T
|
|
|
ENST00000375916.3:c.269+254C>T
(APOM)
|
ENSP00000365081.3:n.269+254C>T
|
|
|
ENST00000375918.6:c.53+254C>T
(APOM)
|
ENSP00000365083.2:n.53+254C>T
|
|
|
ENST00000375920.8:c.53+254C>T
(APOM)
|
ENSP00000365085.4:n.53+254C>T
|
|
|
NM_001256169.1:c.53+254C>T
(APOM)
|
NP_001243098.1:n.53+254C>T
|
|
|
NM_019101.2:c.269+254C>T
(APOM)
|
NP_061974.2:n.269+254C>T
|
|
|
NR_045828.1:n.304+247C>T
(APOM)
|
|
|
|
XM_006715150.2:c.173+247C>T
(APOM)
|
XP_006715213.1:n.173+247C>T
|
|
|
XM_011514895.1:c.-14+3441G>A
(BAG6)
|
XP_011513197.1:n.-14+3441G>A
|
|
|
XM_006715150.3:c.173+247C>T
(APOM)
|
XP_006715213.1:n.173+247C>T
|
|
|
XM_017011279.2:c.-14+3441G>A
(BAG6)
|
XP_016866768.1:n.-14+3441G>A
|
|
|
XM_024446545.1:c.-14+884G>A
(BAG6)
|
XP_024302313.1:n.-14+884G>A
|
|
|
NM_019101.3:c.269+254C>T
(APOM)
MANE Select
|
NP_061974.2:n.269+254C>T
|
|
|
NM_001256169.2:c.53+254C>T
(APOM)
|
NP_001243098.1:n.53+254C>T
|
|
|
NR_045828.2:n.310+247C>T
(APOM)
|
|
|
