ENST00000318602.12:c.2646G>C
(A2M)
MANE Select
|
ENSP00000323929.8:p.Leu882=
|
|
ENST00000318602.11:c.2646G>C
(A2M)
|
ENSP00000323929.7:p.Leu882=
|
|
ENST00000462568.1:n.225G>C
(A2M)
|
|
|
ENST00000543436.2:n.389G>C
(A2M)
|
|
|
ENST00000545828.1:n.348+11576G>C
(A2M)
|
|
|
NM_000014.4:c.2646G>C
(A2M)
|
NP_000005.2:p.Leu882=
|
|
XM_006719056.2:c.2646G>C
(A2M)
|
XP_006719119.1:p.Leu882=
|
|
NM_000014.5:c.2646G>C
(A2M)
|
NP_000005.2:p.Leu882=
|
|
NM_001347423.1:c.2646G>C
(A2M)
|
NP_001334352.1:p.Leu882=
|
|
NM_001347424.1:c.2346G>C
(A2M)
|
NP_001334353.1:p.Leu782=
|
|
NM_001347425.1:c.2196G>C
(A2M)
|
NP_001334354.1:p.Leu732=
|
|
XM_006719056.3:c.2646G>C
(A2M)
|
XP_006719119.1:p.Leu882=
|
|
XM_017018683.1:c.*33+31808C>G
(KLRG1)
|
XP_016874172.1:n.*33+31808C>G
|
|
XM_017018684.1:c.*33+31808C>G
(KLRG1)
|
XP_016874173.1:n.*33+31808C>G
|
|
XM_017018685.1:c.*33+31808C>G
(KLRG1)
|
XP_016874174.1:n.*33+31808C>G
|
|
NM_000014.6:c.2646G>C
(A2M)
MANE Select
|
NP_000005.3:p.Leu882=
|
|
NM_001347423.2:c.2646G>C
(A2M)
|
NP_001334352.2:p.Leu882=
|
|
NM_001347424.2:c.2346G>C
(A2M)
|
NP_001334353.2:p.Leu782=
|
|
NM_001347425.2:c.2196G>C
(A2M)
|
NP_001334354.2:p.Leu732=
|
|