|
ENST00000268251.13:c.*915C>G
(ABAT)
MANE Select
|
ENSP00000268251.8:n.*915C>G
|
|
|
ENST00000268251.12:c.*915C>G
(ABAT)
|
ENSP00000268251.8:n.*915C>G
|
|
|
ENST00000396600.6:c.*915C>G
(ABAT)
|
ENSP00000379845.2:n.*915C>G
|
|
|
ENST00000564869.1:n.32-901G>C
(TMEM186)
|
|
|
|
NM_000663.4:c.*915C>G
(ABAT)
|
NP_000654.2:n.*915C>G
|
|
|
NM_001127448.1:c.*915C>G
(ABAT)
|
NP_001120920.1:n.*915C>G
|
|
|
NM_020686.5:c.*915C>G
(ABAT)
|
NP_065737.2:n.*915C>G
|
|
|
XM_011522400.1:c.*915C>G
(ABAT)
|
XP_011520702.1:n.*915C>G
|
|
|
XM_011522401.1:c.*915C>G
(ABAT)
|
XP_011520703.1:n.*915C>G
|
|
|
XM_011522400.2:c.*915C>G
(ABAT)
|
XP_011520702.1:n.*915C>G
|
|
|
XM_011522401.2:c.*915C>G
(ABAT)
|
XP_011520703.1:n.*915C>G
|
|
|
NM_020686.6:c.*915C>G
(ABAT)
MANE Select
|
NP_065737.2:n.*915C>G
|
|
|
NM_001127448.2:c.*915C>G
(ABAT)
|
NP_001120920.1:n.*915C>G
|
|
|
NM_000663.5:c.*915C>G
(ABAT)
|
NP_000654.2:n.*915C>G
|
|
|
NM_001386600.1:c.*915C>G
(ABAT)
|
NP_001373529.1:n.*915C>G
|
|
|
NM_001386601.1:c.*915C>G
(ABAT)
|
NP_001373530.1:n.*915C>G
|
|
|
NM_001386602.1:c.*915C>G
(ABAT)
|
NP_001373531.1:n.*915C>G
|
|
|
NM_001386603.1:c.*915C>G
(ABAT)
|
NP_001373532.1:n.*915C>G
|
|
|
NM_001386604.1:c.*915C>G
(ABAT)
|
NP_001373533.1:n.*915C>G
|
|
|
NM_001386605.1:c.*915C>G
(ABAT)
|
NP_001373534.1:n.*915C>G
|
|
|
NM_001386606.1:c.*915C>G
(ABAT)
|
NP_001373535.1:n.*915C>G
|
|
|
NM_001386607.1:c.*915C>G
(ABAT)
|
NP_001373536.1:n.*915C>G
|
|
|
NM_001386608.1:c.*915C>G
(ABAT)
|
NP_001373537.1:n.*915C>G
|
|
|
NM_001386609.1:c.*929C>G
(ABAT)
|
NP_001373538.1:n.*929C>G
|
|
|
NM_001386610.1:c.*915C>G
(ABAT)
|
NP_001373539.1:n.*915C>G
|
|
|
NM_001386611.1:c.*915C>G
(ABAT)
|
NP_001373540.1:n.*915C>G
|
|
|
NM_001386612.1:c.*915C>G
(ABAT)
|
NP_001373541.1:n.*915C>G
|
|
|
NM_001386613.1:c.*915C>G
(ABAT)
|
NP_001373542.1:n.*915C>G
|
|
|
NM_001386614.1:c.*915C>G
(ABAT)
|
NP_001373543.1:n.*915C>G
|
|
|
NM_001386615.1:c.*915C>G
(ABAT)
|
NP_001373544.1:n.*915C>G
|
|
|
NM_001386616.1:c.*929C>G
(ABAT)
|
NP_001373545.1:n.*929C>G
|
|
