ENST00000318602.12:c.4264-106G>A
(A2M)
MANE Select
|
ENSP00000323929.8:n.4264-106G>A
|
|
ENST00000318602.11:c.4264-106G>A
(A2M)
|
ENSP00000323929.7:n.4264-106G>A
|
|
ENST00000495442.1:n.8G>A
(A2M)
|
|
|
ENST00000495709.1:n.131G>A
(A2M)
|
|
|
ENST00000543436.2:n.452-1136G>A
(A2M)
|
|
|
NM_000014.4:c.4264-106G>A
(A2M)
|
NP_000005.2:n.4264-106G>A
|
|
XM_006719056.2:c.4264-106G>A
(A2M)
|
XP_006719119.1:n.4264-106G>A
|
|
NM_000014.5:c.4264-106G>A
(A2M)
|
NP_000005.2:n.4264-106G>A
|
|
NM_001347423.1:c.4264-106G>A
(A2M)
|
NP_001334352.1:n.4264-106G>A
|
|
NM_001347424.1:c.3964-106G>A
(A2M)
|
NP_001334353.1:n.3964-106G>A
|
|
NM_001347425.1:c.3814-106G>A
(A2M)
|
NP_001334354.1:n.3814-106G>A
|
|
XM_006719056.3:c.4264-106G>A
(A2M)
|
XP_006719119.1:n.4264-106G>A
|
|
XM_017018683.1:c.*33+10782C>T
(KLRG1)
|
XP_016874172.1:n.*33+10782C>T
|
|
XM_017018684.1:c.*33+10782C>T
(KLRG1)
|
XP_016874173.1:n.*33+10782C>T
|
|
XM_017018685.1:c.*33+10782C>T
(KLRG1)
|
XP_016874174.1:n.*33+10782C>T
|
|
NM_000014.6:c.4264-106G>A
(A2M)
MANE Select
|
NP_000005.3:n.4264-106G>A
|
|
NM_001347423.2:c.4264-106G>A
(A2M)
|
NP_001334352.2:n.4264-106G>A
|
|
NM_001347424.2:c.3964-106G>A
(A2M)
|
NP_001334353.2:n.3964-106G>A
|
|
NM_001347425.2:c.3814-106G>A
(A2M)
|
NP_001334354.2:n.3814-106G>A
|
|