ENST00000375916.4:c.274G>C
(APOM)
MANE Select
|
ENSP00000365081.3:p.Asp92His
|
|
ENST00000375916.3:c.274G>C
(APOM)
|
ENSP00000365081.3:p.Asp92His
|
|
ENST00000375918.6:c.58G>C
(APOM)
|
ENSP00000365083.2:p.Asp20His
|
|
ENST00000375920.8:c.58G>C
(APOM)
|
ENSP00000365085.4:p.Asp20His
|
|
NM_001256169.1:c.58G>C
(APOM)
|
NP_001243098.1:p.Asp20His
|
|
NM_019101.2:c.274G>C
(APOM)
|
NP_061974.2:p.Asp92His
|
|
NR_045828.1:n.309G>C
(APOM)
|
|
|
XM_006715150.2:c.178G>C
(APOM)
|
XP_006715213.1:p.Asp60His
|
|
XM_011514895.1:c.-14+3092C>G
(BAG6)
|
XP_011513197.1:n.-14+3092C>G
|
|
XM_006715150.3:c.178G>C
(APOM)
|
XP_006715213.1:p.Asp60His
|
|
XM_017011279.2:c.-14+3092C>G
(BAG6)
|
XP_016866768.1:n.-14+3092C>G
|
|
XM_024446545.1:c.-14+535C>G
(BAG6)
|
XP_024302313.1:n.-14+535C>G
|
|
NM_019101.3:c.274G>C
(APOM)
MANE Select
|
NP_061974.2:p.Asp92His
|
|
NM_001256169.2:c.58G>C
(APOM)
|
NP_001243098.1:p.Asp20His
|
|
NR_045828.2:n.315G>C
(APOM)
|
|
|