|
ENST00000318602.12:c.18C>T
(A2M)
MANE Select
|
ENSP00000323929.8:p.Leu6=
|
|
|
ENST00000318602.11:c.18C>T
(A2M)
|
ENSP00000323929.7:p.Leu6=
|
|
|
ENST00000404455.2:c.18C>T
(A2M)
|
ENSP00000385710.2:p.Leu6=
|
|
|
ENST00000467091.1:n.230C>T
(A2M)
|
|
|
|
ENST00000497324.1:n.186C>T
(A2M)
|
|
|
|
ENST00000539638.5:c.18C>T
(A2M)
|
ENSP00000445717.1:p.Leu6=
|
|
|
NM_000014.4:c.18C>T
(A2M)
|
NP_000005.2:p.Leu6=
|
|
|
XM_006719056.2:c.18C>T
(A2M)
|
XP_006719119.1:p.Leu6=
|
|
|
NM_000014.5:c.18C>T
(A2M)
|
NP_000005.2:p.Leu6=
|
|
|
NM_001347423.1:c.18C>T
(A2M)
|
NP_001334352.1:p.Leu6=
|
|
|
NM_001347424.1:c.-436C>T
(A2M)
|
NP_001334353.1:n.-436C>T
|
|
|
NM_001347425.1:c.-273C>T
(A2M)
|
NP_001334354.1:n.-273C>T
|
|
|
XM_006719056.3:c.18C>T
(A2M)
|
XP_006719119.1:p.Leu6=
|
|
|
XM_017018683.1:c.*34-9542G>A
(KLRG1)
|
XP_016874172.1:n.*34-9542G>A
|
|
|
XM_017018684.1:c.*34-19254G>A
(KLRG1)
|
XP_016874173.1:n.*34-19254G>A
|
|
|
XM_017018685.1:c.*33+57666G>A
(KLRG1)
|
XP_016874174.1:n.*33+57666G>A
|
|
|
NM_000014.6:c.18C>T
(A2M)
MANE Select
|
NP_000005.3:p.Leu6=
|
|
|
NM_001347423.2:c.18C>T
(A2M)
|
NP_001334352.2:p.Leu6=
|
|
|
NM_001347424.2:c.-436C>T
(A2M)
|
NP_001334353.2:n.-436C>T
|
|
|
NM_001347425.2:c.-273C>T
(A2M)
|
NP_001334354.2:n.-273C>T
|
|
