ENST00000699485.1:c.963G>T
|
ENSP00000514396.1:p.Arg321=
|
|
ENST00000362057.4:c.2619G>T
MANE Select
|
ENSP00000354623.3:p.Arg873=
|
|
ENST00000674036.8:c.1592G>T
|
|
|
ENST00000674048.1:n.2500G>T
|
|
|
ENST00000265134.10:c.1470G>T
|
ENSP00000265134.6:p.Arg490=
|
|
ENST00000362057.3:c.2619G>T
|
ENSP00000354623.3:p.Arg873=
|
|
ENST00000374059.7:c.1566G>T
|
ENSP00000363172.3:p.Arg522=
|
|
NM_001083885.2:c.1470G>T
|
NP_001077354.2:p.Arg490=
|
|
NM_001173425.1:c.2616G>T
|
NP_001166896.1:p.Arg872=
|
|
NM_015404.3:c.2619G>T
|
NP_056219.3:p.Arg873=
|
|
XM_005251897.3:c.1956G>T
|
XP_005251954.2:p.Arg652=
|
|
XM_011518484.1:c.2652G>T
|
XP_011516786.1:p.Arg884=
|
|
XM_011518485.1:c.2652G>T
|
XP_011516787.1:p.Arg884=
|
|
XM_011518486.1:c.2649G>T
|
XP_011516788.1:p.Arg883=
|
|
XM_011518487.1:c.2526G>T
|
XP_011516789.1:p.Arg842=
|
|
XM_011518488.1:c.2409G>T
|
XP_011516790.1:p.Arg803=
|
|
XM_011518495.1:c.1329G>T
|
XP_011516797.1:p.Arg443=
|
|
NM_001346890.1:c.1566G>T
|
NP_001333819.1:p.Arg522=
|
|
XM_011518486.2:c.2649G>T
|
XP_011516788.1:p.Arg883=
|
|
XM_011518487.2:c.2526G>T
|
XP_011516789.1:p.Arg842=
|
|
XM_011518488.2:c.2409G>T
|
XP_011516790.1:p.Arg803=
|
|
NM_015404.4:c.2619G>T
MANE Select
|
NP_056219.3:p.Arg873=
|
|
NM_001173425.2:c.2616G>T
|
NP_001166896.1:p.Arg872=
|
|
NM_001083885.3:c.1470G>T
|
NP_001077354.2:p.Arg490=
|
|