ENST00000209873.9:c.1061A>G
MANE Select
|
ENSP00000209873.4:p.Tyr354Cys
|
|
ENST00000546562.6:n.2125A>G
|
|
|
ENST00000547238.6:n.1697A>G
|
|
|
ENST00000547520.6:n.1055A>G
|
|
|
ENST00000547757.2:c.110A>G
|
ENSP00000448020.2:p.Tyr37Cys
|
|
ENST00000548880.2:n.1511A>G
|
|
|
ENST00000548931.6:c.581A>G
|
ENSP00000457518.1:p.Tyr194Cys
|
|
ENST00000549450.6:n.995A>G
|
|
|
ENST00000552161.6:n.2017A>G
|
|
|
ENST00000672797.1:n.1550A>G
|
|
|
ENST00000672900.1:n.2003A>G
|
|
|
ENST00000209873.8:c.1061A>G
|
ENSP00000209873.4:p.Tyr354Cys
|
|
ENST00000394384.7:c.962A>G
|
ENSP00000377908.3:p.Tyr321Cys
|
|
ENST00000547520.5:n.765A>G
|
|
|
ENST00000548931.5:c.581A>G
|
ENSP00000457518.1:p.Tyr194Cys
|
|
ENST00000550033.5:n.316A>G
|
|
|
ENST00000550286.5:c.689A>G
|
ENSP00000446885.1:p.Tyr230Cys
|
|
ENST00000552876.5:n.1404A>G
|
|
|
NM_001173466.1:c.962A>G
|
NP_001166937.1:p.Tyr321Cys
|
|
NM_015665.5:c.1061A>G
|
NP_056480.1:p.Tyr354Cys
|
|
XM_006719617.2:c.1076A>G
|
XP_006719680.1:p.Tyr359Cys
|
|
XM_011538777.1:c.1076A>G
|
XP_011537079.1:p.Tyr359Cys
|
|
XM_011538778.1:c.1061A>G
|
XP_011537080.1:p.Tyr354Cys
|
|
XM_011538779.1:c.977A>G
|
XP_011537081.1:p.Tyr326Cys
|
|
XM_011538780.1:c.962A>G
|
XP_011537082.1:p.Tyr321Cys
|
|
XM_011538781.1:c.410A>G
|
XP_011537083.1:p.Tyr137Cys
|
|
XM_011538778.2:c.1061A>G
|
XP_011537080.1:p.Tyr354Cys
|
|
XM_011538780.2:c.962A>G
|
XP_011537082.1:p.Tyr321Cys
|
|
XR_001748875.2:n.1118A>G
|
|
|
NM_015665.6:c.1061A>G
MANE Select
|
NP_056480.1:p.Tyr354Cys
|
|
NM_001173466.2:c.962A>G
|
NP_001166937.1:p.Tyr321Cys
|
|