ENST00000265631.10:c.1694G>A
MANE Select
|
ENSP00000265631.6:p.Cys565Tyr
|
|
ENST00000265631.9:c.1694G>A
|
ENSP00000265631.5:p.Cys565Tyr
|
|
ENST00000416240.6:c.1697G>A
|
ENSP00000400101.2:p.Cys566Tyr
|
|
ENST00000494085.1:n.104G>A
|
|
|
NM_001160210.1:c.1697G>A
|
NP_001153682.1:p.Cys566Tyr
|
|
NM_014251.2:c.1694G>A
|
NP_055066.1:p.Cys565Tyr
|
|
NR_027662.1:n.1769G>A
|
|
|
XM_006715831.2:c.1727G>A
|
XP_006715894.1:p.Cys576Tyr
|
|
XM_011515728.1:c.842G>A
|
XP_011514030.1:p.Cys281Tyr
|
|
XM_006715831.4:c.1727G>A
|
XP_006715894.1:p.Cys576Tyr
|
|
XM_017011663.1:c.1685G>A
|
XP_016867152.1:p.Cys562Tyr
|
|
XM_017011664.2:c.842G>A
|
XP_016867153.1:p.Cys281Tyr
|
|
XM_017011665.1:c.842G>A
|
XP_016867154.1:p.Cys281Tyr
|
|
XR_001744525.2:n.1940G>A
|
|
|
XR_002956405.1:n.2498G>A
|
|
|
NM_014251.3:c.1694G>A
MANE Select
|
NP_055066.1:p.Cys565Tyr
|
|
NR_027662.2:n.1720G>A
|
|
|
NM_001160210.2:c.1697G>A
|
NP_001153682.1:p.Cys566Tyr
|
|