ENST00000318602.12:c.4365G>C
(A2M)
MANE Select
|
ENSP00000323929.8:p.Thr1455=
|
|
ENST00000318602.11:c.4365G>C
(A2M)
|
ENSP00000323929.7:p.Thr1455=
|
|
ENST00000495442.1:n.215G>C
(A2M)
|
|
|
ENST00000495709.1:n.338G>C
(A2M)
|
|
|
ENST00000543436.2:n.452-929G>C
(A2M)
|
|
|
NM_000014.4:c.4365G>C
(A2M)
|
NP_000005.2:p.Thr1455=
|
|
XM_006719056.2:c.4365G>C
(A2M)
|
XP_006719119.1:p.Thr1455=
|
|
NM_000014.5:c.4365G>C
(A2M)
|
NP_000005.2:p.Thr1455=
|
|
NM_001347423.1:c.4365G>C
(A2M)
|
NP_001334352.1:p.Thr1455=
|
|
NM_001347424.1:c.4065G>C
(A2M)
|
NP_001334353.1:p.Thr1355=
|
|
NM_001347425.1:c.3915G>C
(A2M)
|
NP_001334354.1:p.Thr1305=
|
|
XM_006719056.3:c.4365G>C
(A2M)
|
XP_006719119.1:p.Thr1455=
|
|
XM_017018683.1:c.*33+10575C>G
(KLRG1)
|
XP_016874172.1:n.*33+10575C>G
|
|
XM_017018684.1:c.*33+10575C>G
(KLRG1)
|
XP_016874173.1:n.*33+10575C>G
|
|
XM_017018685.1:c.*33+10575C>G
(KLRG1)
|
XP_016874174.1:n.*33+10575C>G
|
|
NM_000014.6:c.4365G>C
(A2M)
MANE Select
|
NP_000005.3:p.Thr1455=
|
|
NM_001347423.2:c.4365G>C
(A2M)
|
NP_001334352.2:p.Thr1455=
|
|
NM_001347424.2:c.4065G>C
(A2M)
|
NP_001334353.2:p.Thr1355=
|
|
NM_001347425.2:c.3915G>C
(A2M)
|
NP_001334354.2:p.Thr1305=
|
|