ENST00000209873.9:c.972G>A
MANE Select
|
ENSP00000209873.4:p.Trp324Ter
|
|
ENST00000546393.7:n.1817G>A
|
|
|
ENST00000546562.6:n.2036G>A
|
|
|
ENST00000547238.6:n.1608G>A
|
|
|
ENST00000547520.6:n.966G>A
|
|
|
ENST00000547757.2:c.21G>A
|
ENSP00000448020.2:p.Trp7Ter
|
|
ENST00000548880.2:n.1422G>A
|
|
|
ENST00000548931.6:c.492G>A
|
ENSP00000457518.1:p.Trp164Ter
|
|
ENST00000549450.6:n.906G>A
|
|
|
ENST00000552161.6:n.1928G>A
|
|
|
ENST00000672797.1:n.1425G>A
|
|
|
ENST00000672900.1:n.1770G>A
|
|
|
ENST00000209873.8:c.972G>A
|
ENSP00000209873.4:p.Trp324Ter
|
|
ENST00000394384.7:c.873G>A
|
ENSP00000377908.3:p.Trp291Ter
|
|
ENST00000546572.1:n.560G>A
|
|
|
ENST00000547520.5:n.676G>A
|
|
|
ENST00000548931.5:c.492G>A
|
ENSP00000457518.1:p.Trp164Ter
|
|
ENST00000550033.5:n.227G>A
|
|
|
ENST00000550286.5:c.600G>A
|
ENSP00000446885.1:p.Trp200Ter
|
|
ENST00000552876.5:n.1315G>A
|
|
|
NM_001173466.1:c.873G>A
|
NP_001166937.1:p.Trp291Ter
|
|
NM_015665.5:c.972G>A
|
NP_056480.1:p.Trp324Ter
|
|
XM_006719617.2:c.987G>A
|
XP_006719680.1:p.Trp329Ter
|
|
XM_006719619.2:c.987G>A
|
XP_006719682.1:p.Trp329Ter
|
|
XM_011538777.1:c.987G>A
|
XP_011537079.1:p.Trp329Ter
|
|
XM_011538778.1:c.972G>A
|
XP_011537080.1:p.Trp324Ter
|
|
XM_011538779.1:c.888G>A
|
XP_011537081.1:p.Trp296Ter
|
|
XM_011538780.1:c.873G>A
|
XP_011537082.1:p.Trp291Ter
|
|
XM_011538781.1:c.321G>A
|
XP_011537083.1:p.Trp107Ter
|
|
XM_011538778.2:c.972G>A
|
XP_011537080.1:p.Trp324Ter
|
|
XM_011538780.2:c.873G>A
|
XP_011537082.1:p.Trp291Ter
|
|
XR_001748875.2:n.993G>A
|
|
|
NM_015665.6:c.972G>A
MANE Select
|
NP_056480.1:p.Trp324Ter
|
|
NM_001173466.2:c.873G>A
|
NP_001166937.1:p.Trp291Ter
|
|