ENST00000546910.6:c.*2725A>G
(CLEC5A)
MANE Select
|
ENSP00000449999.1:n.*2725A>G
|
|
ENST00000465654.5:c.-179-18442T>C
(MGAM)
|
ENSP00000419372.1:n.-179-18442T>C
|
|
ENST00000497554.1:n.37-2398T>C
(MGAM)
|
|
|
ENST00000546910.5:c.*2725A>G
(CLEC5A)
|
ENSP00000449999.1:n.*2725A>G
|
|
NM_001301167.1:c.*2725A>G
(CLEC5A)
|
NP_001288096.1:n.*2725A>G
|
|
NM_013252.2:c.*2725A>G
(CLEC5A)
|
NP_037384.1:n.*2725A>G
|
|
XM_011515783.1:c.*24+7535T>C
(OR9A4)
|
XP_011514085.1:n.*24+7535T>C
|
|
XM_011515995.1:c.*2725A>G
(CLEC5A)
|
XP_011514297.1:n.*2725A>G
|
|
XR_927428.1:n.2676A>G
(CLEC5A)
|
|
|
XM_011515995.2:c.*2725A>G
(CLEC5A)
|
XP_011514297.1:n.*2725A>G
|
|
XM_017011915.1:c.*2725A>G
(CLEC5A)
|
XP_016867404.1:n.*2725A>G
|
|
XM_017011917.1:c.*2793A>G
(CLEC5A)
|
XP_016867406.1:n.*2793A>G
|
|
NM_013252.3:c.*2725A>G
(CLEC5A)
MANE Select
|
NP_037384.1:n.*2725A>G
|
|
NM_001301167.2:c.*2725A>G
(CLEC5A)
|
NP_001288096.1:n.*2725A>G
|
|