ENST00000295408.9:c.2262C>A
MANE Select
|
ENSP00000295408.4:p.Tyr754Ter
|
|
ENST00000295408.8:c.2262C>A
|
ENSP00000295408.4:p.Tyr754Ter
|
|
ENST00000409780.5:c.1734C>A
|
ENSP00000387277.1:p.Tyr578Ter
|
|
ENST00000421804.6:c.2262C>A
|
ENSP00000389152.2:p.Tyr754Ter
|
|
ENST00000439966.5:c.*1735C>A
|
ENSP00000402129.1:n.*1735C>A
|
|
ENST00000449344.2:c.234C>A
|
ENSP00000412660.2:p.Tyr78Ter
|
|
ENST00000616902.4:c.1218C>A
|
ENSP00000482824.1:p.Tyr406Ter
|
|
NM_006343.2:c.2262C>A
|
NP_006334.2:p.Tyr754Ter
|
|
XM_005263565.3:c.2262C>A
|
XP_005263622.1:p.Tyr754Ter
|
|
XM_011510490.1:c.2073C>A
|
XP_011508792.1:p.Tyr691Ter
|
|
XM_011510491.1:c.1047C>A
|
XP_011508793.1:p.Tyr349Ter
|
|
XM_005263565.4:c.2262C>A
|
XP_005263622.1:p.Tyr754Ter
|
|
XM_011510490.3:c.2073C>A
|
XP_011508792.1:p.Tyr691Ter
|
|
XM_017003164.1:c.2073C>A
|
XP_016858653.1:p.Tyr691Ter
|
|
XM_017003165.2:c.1047C>A
|
XP_016858654.1:p.Tyr349Ter
|
|
NM_006343.3:c.2262C>A
MANE Select
|
NP_006334.2:p.Tyr754Ter
|
|