ENST00000318602.12:c.-1C>G
(A2M)
MANE Select
|
ENSP00000323929.8:n.-1C>G
|
|
ENST00000318602.11:c.-1C>G
(A2M)
|
ENSP00000323929.7:n.-1C>G
|
|
ENST00000404455.2:c.-1C>G
(A2M)
|
ENSP00000385710.2:n.-1C>G
|
|
ENST00000467091.1:n.212C>G
(A2M)
|
|
|
ENST00000497324.1:n.168C>G
(A2M)
|
|
|
ENST00000539638.5:c.-1C>G
(A2M)
|
ENSP00000445717.1:n.-1C>G
|
|
NM_000014.4:c.-1C>G
(A2M)
|
NP_000005.2:n.-1C>G
|
|
XM_006719056.2:c.-1C>G
(A2M)
|
XP_006719119.1:n.-1C>G
|
|
NM_000014.5:c.-1C>G
(A2M)
|
NP_000005.2:n.-1C>G
|
|
NM_001347423.1:c.-1C>G
(A2M)
|
NP_001334352.1:n.-1C>G
|
|
NM_001347424.1:c.-454C>G
(A2M)
|
NP_001334353.1:n.-454C>G
|
|
NM_001347425.1:c.-291C>G
(A2M)
|
NP_001334354.1:n.-291C>G
|
|
XM_006719056.3:c.-1C>G
(A2M)
|
XP_006719119.1:n.-1C>G
|
|
XM_017018683.1:c.*34-9524G>C
(KLRG1)
|
XP_016874172.1:n.*34-9524G>C
|
|
XM_017018684.1:c.*34-19236G>C
(KLRG1)
|
XP_016874173.1:n.*34-19236G>C
|
|
XM_017018685.1:c.*33+57684G>C
(KLRG1)
|
XP_016874174.1:n.*33+57684G>C
|
|
NM_000014.6:c.-1C>G
(A2M)
MANE Select
|
NP_000005.3:n.-1C>G
|
|
NM_001347423.2:c.-1C>G
(A2M)
|
NP_001334352.2:n.-1C>G
|
|
NM_001347424.2:c.-454C>G
(A2M)
|
NP_001334353.2:n.-454C>G
|
|
NM_001347425.2:c.-291C>G
(A2M)
|
NP_001334354.2:n.-291C>G
|
|