ENST00000175238.10:c.1912A>C
(ADAM7)
MANE Select
|
ENSP00000175238.5:p.Asn638His
|
|
ENST00000380789.5:c.1912A>C
(ADAM7)
|
ENSP00000370166.1:p.Asn638His
|
|
ENST00000520720.1:c.1228A>C
(ADAM7)
|
ENSP00000430400.1:p.Asn410His
|
|
NM_003817.3:c.1912A>C
(ADAM7)
|
NP_003808.2:p.Asn638His
|
|
NR_125808.1:n.79+49235T>G
(ADAM7-AS1)
|
|
|
NR_125809.1:n.447-7145T>G
(ADAM7-AS2)
|
|
|
XM_005273668.2:c.1912A>C
(ADAM7)
|
XP_005273725.1:p.Asn638His
|
|
XM_005273669.2:c.1912A>C
(ADAM7)
|
XP_005273726.1:p.Asn638His
|
|
XM_005273670.1:c.1912A>C
(ADAM7)
|
XP_005273727.1:p.Asn638His
|
|
XM_005273671.2:c.1912A>C
(ADAM7)
|
XP_005273728.1:p.Asn638His
|
|
XM_005273672.2:c.1843-873A>C
(ADAM7)
|
XP_005273729.1:n.1843-873A>C
|
|
XM_005273673.1:c.1912A>C
(ADAM7)
|
XP_005273730.1:p.Asn638His
|
|
XM_017013943.1:c.1912A>C
(ADAM7)
|
XP_016869432.1:p.Asn638His
|
|
NM_003817.4:c.1912A>C
(ADAM7)
MANE Select
|
NP_003808.2:p.Asn638His
|
|