ENST00000286657.10:c.1688G>T
MANE Select
|
ENSP00000286657.4:p.Cys563Phe
|
|
ENST00000286657.8:c.1688G>T
|
ENSP00000286657.4:p.Cys563Phe
|
|
ENST00000622135.1:c.1688G>T
|
ENSP00000480055.1:p.Cys563Phe
|
|
NM_014243.2:c.1688G>T
|
NP_055058.2:p.Cys563Phe
|
|
XM_011532421.1:c.1631G>T
|
XP_011530723.1:p.Cys544Phe
|
|
XM_011532422.1:c.1604G>T
|
XP_011530724.1:p.Cys535Phe
|
|
XM_011532423.1:c.1046G>T
|
XP_011530725.1:p.Cys349Phe
|
|
XM_011532424.1:c.956G>T
|
XP_011530726.1:p.Cys319Phe
|
|
XM_011532421.2:c.1631G>T
|
XP_011530723.1:p.Cys544Phe
|
|
XM_011532422.3:c.1604G>T
|
XP_011530724.1:p.Cys535Phe
|
|
NM_014243.3:c.1688G>T
MANE Select
|
NP_055058.2:p.Cys563Phe
|
|