ENST00000286657.10:c.1733G>A
MANE Select
|
ENSP00000286657.4:p.Cys578Tyr
|
|
ENST00000286657.8:c.1733G>A
|
ENSP00000286657.4:p.Cys578Tyr
|
|
ENST00000622135.1:c.1733G>A
|
ENSP00000480055.1:p.Cys578Tyr
|
|
NM_014243.2:c.1733G>A
|
NP_055058.2:p.Cys578Tyr
|
|
XM_011532421.1:c.1676G>A
|
XP_011530723.1:p.Cys559Tyr
|
|
XM_011532422.1:c.1649G>A
|
XP_011530724.1:p.Cys550Tyr
|
|
XM_011532423.1:c.1091G>A
|
XP_011530725.1:p.Cys364Tyr
|
|
XM_011532424.1:c.1001G>A
|
XP_011530726.1:p.Cys334Tyr
|
|
XM_011532421.2:c.1676G>A
|
XP_011530723.1:p.Cys559Tyr
|
|
XM_011532422.3:c.1649G>A
|
XP_011530724.1:p.Cys550Tyr
|
|
NM_014243.3:c.1733G>A
MANE Select
|
NP_055058.2:p.Cys578Tyr
|
|