ENST00000209873.9:c.1007G>C
MANE Select
|
ENSP00000209873.4:p.Trp336Ser
|
|
ENST00000546393.7:n.1852G>C
|
|
|
ENST00000546562.6:n.2071G>C
|
|
|
ENST00000547238.6:n.1643G>C
|
|
|
ENST00000547520.6:n.1001G>C
|
|
|
ENST00000547757.2:c.56G>C
|
ENSP00000448020.2:p.Trp19Ser
|
|
ENST00000548880.2:n.1457G>C
|
|
|
ENST00000548931.6:c.527G>C
|
ENSP00000457518.1:p.Trp176Ser
|
|
ENST00000549450.6:n.941G>C
|
|
|
ENST00000552161.6:n.1963G>C
|
|
|
ENST00000672797.1:n.1496G>C
|
|
|
ENST00000672900.1:n.1949G>C
|
|
|
ENST00000209873.8:c.1007G>C
|
ENSP00000209873.4:p.Trp336Ser
|
|
ENST00000394384.7:c.908G>C
|
ENSP00000377908.3:p.Trp303Ser
|
|
ENST00000547520.5:n.711G>C
|
|
|
ENST00000548931.5:c.527G>C
|
ENSP00000457518.1:p.Trp176Ser
|
|
ENST00000550033.5:n.262G>C
|
|
|
ENST00000550286.5:c.635G>C
|
ENSP00000446885.1:p.Trp212Ser
|
|
ENST00000552876.5:n.1350G>C
|
|
|
NM_001173466.1:c.908G>C
|
NP_001166937.1:p.Trp303Ser
|
|
NM_015665.5:c.1007G>C
|
NP_056480.1:p.Trp336Ser
|
|
XM_006719617.2:c.1022G>C
|
XP_006719680.1:p.Trp341Ser
|
|
XM_006719619.2:c.*17G>C
|
XP_006719682.1:n.*17G>C
|
|
XM_011538777.1:c.1022G>C
|
XP_011537079.1:p.Trp341Ser
|
|
XM_011538778.1:c.1007G>C
|
XP_011537080.1:p.Trp336Ser
|
|
XM_011538779.1:c.923G>C
|
XP_011537081.1:p.Trp308Ser
|
|
XM_011538780.1:c.908G>C
|
XP_011537082.1:p.Trp303Ser
|
|
XM_011538781.1:c.356G>C
|
XP_011537083.1:p.Trp119Ser
|
|
XM_011538778.2:c.1007G>C
|
XP_011537080.1:p.Trp336Ser
|
|
XM_011538780.2:c.908G>C
|
XP_011537082.1:p.Trp303Ser
|
|
XR_001748875.2:n.1064G>C
|
|
|
NM_015665.6:c.1007G>C
MANE Select
|
NP_056480.1:p.Trp336Ser
|
|
NM_001173466.2:c.908G>C
|
NP_001166937.1:p.Trp303Ser
|
|