ENST00000478630.2:n.2937C>T
|
|
|
ENST00000674112.2:c.*59C>T
|
ENSP00000501166.2:n.*59C>T
|
|
ENST00000683242.1:n.1264C>T
|
|
|
ENST00000685042.1:c.*1373C>T
|
ENSP00000509871.1:n.*1373C>T
|
|
ENST00000686442.1:n.5595C>T
|
|
|
ENST00000687225.1:c.*3003C>T
|
ENSP00000509364.1:n.*3003C>T
|
|
ENST00000688302.1:n.5138C>T
|
|
|
ENST00000689256.1:n.5294C>T
|
|
|
ENST00000690231.1:c.4717C>T
|
ENSP00000508461.1:p.Arg1573Ter
|
|
ENST00000692002.1:c.742C>T
|
ENSP00000508567.1:p.Arg248Ter
|
|
ENST00000265348.9:c.4717C>T
MANE Select
|
ENSP00000265348.4:p.Arg1573Ter
|
|
ENST00000673725.1:c.2577C>T
|
|
|
ENST00000673753.1:n.5545C>T
|
|
|
ENST00000674100.1:c.4813C>T
|
ENSP00000501292.1:p.Arg1605Ter
|
|
ENST00000674112.1:c.3198C>T
|
|
|
ENST00000674134.1:c.4813C>T
|
ENSP00000501068.1:p.Arg1605Ter
|
|
ENST00000265348.7:c.4717C>T
|
ENSP00000265348.3:p.Arg1573Ter
|
|
ENST00000535468.1:c.4969C>T
|
ENSP00000438788.1:p.Arg1657Ter
|
|
NM_001168370.1:c.4969C>T
|
NP_001161842.1:p.Arg1657Ter
|
|
NM_014780.4:c.4717C>T
|
NP_055595.2:p.Arg1573Ter
|
|
XM_005249503.1:c.4873C>T
|
XP_005249560.1:p.Arg1625Ter
|
|
XM_006715285.1:c.4825C>T
|
XP_006715348.1:p.Arg1609Ter
|
|
XM_011515019.1:c.4981C>T
|
XP_011513321.1:p.Arg1661Ter
|
|
XM_011515020.1:c.4885C>T
|
XP_011513322.1:p.Arg1629Ter
|
|
XM_011515021.1:c.2590C>T
|
XP_011513323.1:p.Arg864Ter
|
|
XM_005249503.3:c.4873C>T
|
XP_005249560.1:p.Arg1625Ter
|
|
XM_006715285.2:c.4825C>T
|
XP_006715348.1:p.Arg1609Ter
|
|
XM_011515019.2:c.4981C>T
|
XP_011513321.1:p.Arg1661Ter
|
|
XM_011515020.2:c.4885C>T
|
XP_011513322.1:p.Arg1629Ter
|
|
XM_017011533.1:c.5008C>T
|
XP_016867022.1:p.Arg1670Ter
|
|
XM_017011534.1:c.4996C>T
|
XP_016867023.1:p.Arg1666Ter
|
|
XM_017011535.1:c.4912C>T
|
XP_016867024.1:p.Arg1638Ter
|
|
XM_017011536.2:c.4852C>T
|
XP_016867025.1:p.Arg1618Ter
|
|
XM_017011537.2:c.4813C>T
|
XP_016867026.1:p.Arg1605Ter
|
|
XM_017011538.2:c.4756C>T
|
XP_016867027.1:p.Arg1586Ter
|
|
XM_017011539.2:c.4729C>T
|
XP_016867028.1:p.Arg1577Ter
|
|
NM_001168370.2:c.4813C>T
|
NP_001161842.2:p.Arg1605Ter
|
|
NM_001374872.1:c.4813C>T
|
NP_001361801.1:p.Arg1605Ter
|
|
NM_001374873.1:c.4729C>T
|
NP_001361802.1:p.Arg1577Ter
|
|
NM_001374874.1:c.4714C>T
|
NP_001361803.1:p.Arg1572Ter
|
|
NM_014780.5:c.4717C>T
MANE Select
|
NP_055595.2:p.Arg1573Ter
|
|