ENST00000369798.7:c.2089G>T
MANE Select
|
ENSP00000358813.2:p.Asp697Tyr
|
|
ENST00000230510.7:c.2086G>T
|
ENSP00000230510.3:p.Asp696Tyr
|
|
ENST00000369798.6:c.2089G>T
|
ENSP00000358813.2:p.Asp697Tyr
|
|
ENST00000504590.1:n.454G>T
|
|
|
ENST00000509894.5:c.2086G>T
|
ENSP00000422936.1:p.Asp696Tyr
|
|
NM_001166691.1:c.2086G>T
|
NP_001160163.1:p.Asp696Tyr
|
|
NM_003318.4:c.2089G>T
|
NP_003309.2:p.Asp697Tyr
|
|
XM_011536099.1:c.2089G>T
|
XP_011534401.1:p.Asp697Tyr
|
|
XM_011536100.1:c.2086G>T
|
XP_011534402.1:p.Asp696Tyr
|
|
XM_011536099.3:c.2089G>T
|
XP_011534401.1:p.Asp697Tyr
|
|
XM_011536100.3:c.2086G>T
|
XP_011534402.1:p.Asp696Tyr
|
|
XM_017011242.2:c.1924G>T
|
XP_016866731.1:p.Asp642Tyr
|
|
NM_003318.5:c.2089G>T
MANE Select
|
NP_003309.2:p.Asp697Tyr
|
|
NM_001166691.2:c.2086G>T
|
NP_001160163.1:p.Asp696Tyr
|
|