ENST00000403665.7:c.972C>G
MANE Select
|
ENSP00000384957.2:p.Ala324=
|
|
ENST00000264692.8:c.810C>G
|
ENSP00000264692.5:p.Ala270=
|
|
ENST00000403665.6:c.972C>G
|
ENSP00000384957.2:p.Ala324=
|
|
ENST00000452239.1:c.419C>G
|
|
|
NM_000128.3:c.972C>G , LRG_583t1:c.972C>G
|
NP_000119.1:p.Ala324=
|
|
XM_005262821.2:c.972C>G
|
XP_005262878.1:p.Ala324=
|
|
XM_005262822.2:c.972C>G
|
XP_005262879.1:p.Ala324=
|
|
XM_005262823.2:c.702C>G
|
XP_005262880.1:p.Ala234=
|
|
XM_005262824.1:c.972C>G
|
XP_005262881.1:p.Ala324=
|
|
XM_006714137.1:c.924C>G
|
XP_006714200.1:p.Ala308=
|
|
XR_938706.1:n.1324C>G
|
|
|
XR_938707.1:n.1324C>G
|
|
|
XM_005262821.4:c.972C>G
|
XP_005262878.1:p.Ala324=
|
|
XM_005262822.4:c.972C>G
|
XP_005262879.1:p.Ala324=
|
|
XM_005262823.4:c.702C>G
|
XP_005262880.1:p.Ala234=
|
|
XM_006714137.3:c.924C>G
|
XP_006714200.1:p.Ala308=
|
|
XM_017007884.2:c.972C>G
|
XP_016863373.1:p.Ala324=
|
|
XM_017007885.2:c.972C>G
|
XP_016863374.1:p.Ala324=
|
|
XM_017007886.2:c.972C>G
|
XP_016863375.1:p.Ala324=
|
|
XR_001741172.2:n.1305C>G
|
|
|
NM_000128.4:c.972C>G
MANE Select
|
NP_000119.1:p.Ala324=
|
|