ENST00000256412.8:c.1323G>A
(ADAMDEC1)
MANE Select
|
ENSP00000256412.4:p.Glu441=
|
|
ENST00000520193.1:c.1413G>A
(ADAMDEC1)
|
ENSP00000431008.1:n.1413G>A
|
|
ENST00000522298.1:c.1086G>A
(ADAMDEC1)
|
ENSP00000428993.1:p.Glu362=
|
|
NM_001145271.1:c.1086G>A
(ADAMDEC1)
|
NP_001138743.1:p.Glu362=
|
|
NM_001145272.1:c.1086G>A
(ADAMDEC1)
|
NP_001138744.1:p.Glu362=
|
|
NM_014479.3:c.1323G>A
(ADAMDEC1)
MANE Select
|
NP_055294.1:p.Glu441=
|
|
NR_125808.1:n.80-16014C>T
(ADAM7-AS1)
|
|
|
XR_428306.1:n.1331G>A
(ADAMDEC1)
|
|
|
NR_156422.1:n.1543G>A
(ADAMDEC1)
|
|
|
NM_001145271.2:c.1086G>A
(ADAMDEC1)
|
NP_001138743.1:p.Glu362=
|
|
NM_001145272.2:c.1086G>A
(ADAMDEC1)
|
NP_001138744.1:p.Glu362=
|
|
NR_156422.2:n.1323G>A
(ADAMDEC1)
|
|
|