ENST00000546910.6:c.*2719T>A
(CLEC5A)
MANE Select
|
ENSP00000449999.1:n.*2719T>A
|
|
ENST00000465654.5:c.-179-18436A>T
(MGAM)
|
ENSP00000419372.1:n.-179-18436A>T
|
|
ENST00000497554.1:n.37-2392A>T
(MGAM)
|
|
|
ENST00000546910.5:c.*2719T>A
(CLEC5A)
|
ENSP00000449999.1:n.*2719T>A
|
|
NM_001301167.1:c.*2719T>A
(CLEC5A)
|
NP_001288096.1:n.*2719T>A
|
|
NM_013252.2:c.*2719T>A
(CLEC5A)
|
NP_037384.1:n.*2719T>A
|
|
XM_011515783.1:c.*24+7541A>T
(OR9A4)
|
XP_011514085.1:n.*24+7541A>T
|
|
XM_011515995.1:c.*2719T>A
(CLEC5A)
|
XP_011514297.1:n.*2719T>A
|
|
XR_927428.1:n.2670T>A
(CLEC5A)
|
|
|
XM_011515995.2:c.*2719T>A
(CLEC5A)
|
XP_011514297.1:n.*2719T>A
|
|
XM_017011915.1:c.*2719T>A
(CLEC5A)
|
XP_016867404.1:n.*2719T>A
|
|
XM_017011917.1:c.*2787T>A
(CLEC5A)
|
XP_016867406.1:n.*2787T>A
|
|
NM_013252.3:c.*2719T>A
(CLEC5A)
MANE Select
|
NP_037384.1:n.*2719T>A
|
|
NM_001301167.2:c.*2719T>A
(CLEC5A)
|
NP_001288096.1:n.*2719T>A
|
|