ENST00000286657.10:c.1685C>A
MANE Select
|
ENSP00000286657.4:p.Ser562Tyr
|
|
ENST00000286657.8:c.1685C>A
|
ENSP00000286657.4:p.Ser562Tyr
|
|
ENST00000622135.1:c.1685C>A
|
ENSP00000480055.1:p.Ser562Tyr
|
|
NM_014243.2:c.1685C>A
|
NP_055058.2:p.Ser562Tyr
|
|
XM_011532421.1:c.1628C>A
|
XP_011530723.1:p.Ser543Tyr
|
|
XM_011532422.1:c.1601C>A
|
XP_011530724.1:p.Ser534Tyr
|
|
XM_011532423.1:c.1043C>A
|
XP_011530725.1:p.Ser348Tyr
|
|
XM_011532424.1:c.953C>A
|
XP_011530726.1:p.Ser318Tyr
|
|
XM_011532421.2:c.1628C>A
|
XP_011530723.1:p.Ser543Tyr
|
|
XM_011532422.3:c.1601C>A
|
XP_011530724.1:p.Ser534Tyr
|
|
NM_014243.3:c.1685C>A
MANE Select
|
NP_055058.2:p.Ser562Tyr
|
|