ENST00000299314.12:c.473A>G
MANE Select
|
ENSP00000299314.7:p.Tyr158Cys
|
|
ENST00000299314.11:c.473A>G
|
ENSP00000299314.7:p.Tyr158Cys
|
|
ENST00000549940.5:c.473A>G
|
ENSP00000449150.1:p.Tyr158Cys
|
|
ENST00000550352.1:n.267A>G
|
|
|
ENST00000552681.1:c.107A>G
|
ENSP00000449217.1:p.Tyr36Cys
|
|
NM_024312.4:c.473A>G
|
NP_077288.2:p.Tyr158Cys
|
|
XM_006719593.2:c.473A>G
|
XP_006719656.1:p.Tyr158Cys
|
|
XM_011538731.1:c.392A>G
|
XP_011537033.1:p.Tyr131Cys
|
|
XM_006719593.3:c.473A>G
|
XP_006719656.1:p.Tyr158Cys
|
|
XM_011538731.2:c.392A>G
|
XP_011537033.1:p.Tyr131Cys
|
|
XM_017019961.1:c.257A>G
|
XP_016875450.1:p.Tyr86Cys
|
|
XM_017019962.2:c.-878A>G
|
XP_016875451.1:n.-878A>G
|
|
NM_024312.5:c.473A>G
MANE Select
|
NP_077288.2:p.Tyr158Cys
|
|