ENST00000209873.9:c.1421G>C
MANE Select
|
ENSP00000209873.4:p.Trp474Ser
|
|
ENST00000546562.6:n.2485G>C
|
|
|
ENST00000547238.6:n.2057G>C
|
|
|
ENST00000547520.6:n.1537G>C
|
|
|
ENST00000547757.2:c.*339G>C
|
ENSP00000448020.2:n.*339G>C
|
|
ENST00000548880.2:n.1871G>C
|
|
|
ENST00000548931.6:c.856G>C
|
ENSP00000457518.1:p.Gly286Arg
|
|
ENST00000549450.6:n.1355G>C
|
|
|
ENST00000552161.6:n.2499G>C
|
|
|
ENST00000672797.1:n.1910G>C
|
|
|
ENST00000209873.8:c.1421G>C
|
ENSP00000209873.4:p.Trp474Ser
|
|
ENST00000394384.7:c.1322G>C
|
ENSP00000377908.3:p.Trp441Ser
|
|
ENST00000548931.5:c.856G>C
|
ENSP00000457518.1:p.Gly286Arg
|
|
ENST00000550286.5:c.1049G>C
|
ENSP00000446885.1:p.Trp350Ser
|
|
ENST00000552876.5:n.1764G>C
|
|
|
NM_001173466.1:c.1322G>C
|
NP_001166937.1:p.Trp441Ser
|
|
NM_015665.5:c.1421G>C
|
NP_056480.1:p.Trp474Ser
|
|
XM_006719617.2:c.1436G>C
|
XP_006719680.1:p.Trp479Ser
|
|
XM_011538777.1:c.1478G>C
|
XP_011537079.1:p.Trp493Ser
|
|
XM_011538778.1:c.1463G>C
|
XP_011537080.1:p.Trp488Ser
|
|
XM_011538779.1:c.1379G>C
|
XP_011537081.1:p.Trp460Ser
|
|
XM_011538780.1:c.1364G>C
|
XP_011537082.1:p.Trp455Ser
|
|
XM_011538781.1:c.812G>C
|
XP_011537083.1:p.Trp271Ser
|
|
XM_011538778.2:c.1463G>C
|
XP_011537080.1:p.Trp488Ser
|
|
XM_011538780.2:c.1364G>C
|
XP_011537082.1:p.Trp455Ser
|
|
XR_001748875.2:n.1478G>C
|
|
|
NM_015665.6:c.1421G>C
MANE Select
|
NP_056480.1:p.Trp474Ser
|
|
NM_001173466.2:c.1322G>C
|
NP_001166937.1:p.Trp441Ser
|
|