ENST00000269571.10:c.3690G>T
MANE Select
|
ENSP00000269571.4:p.Arg1230=
|
|
ENST00000269571.9:c.3690G>T
|
ENSP00000269571.4:p.Arg1230=
|
|
ENST00000406381.6:c.3600G>T
|
ENSP00000385185.2:p.Arg1200=
|
|
ENST00000445658.6:c.2862G>T
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ENSP00000404047.2:p.Arg954=
|
|
ENST00000541774.5:c.3645G>T
|
ENSP00000446466.1:p.Arg1215=
|
|
ENST00000578373.5:c.*3480G>T
|
ENSP00000463427.1:n.*3480G>T
|
|
ENST00000584450.5:c.*269G>T
|
ENSP00000463714.1:n.*269G>T
|
|
ENST00000584601.5:c.3600G>T
|
ENSP00000462438.1:p.Arg1200=
|
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NM_001005862.2:c.3600G>T , LRG_724t1:c.3600G>T
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NP_001005862.1:p.Arg1200=
|
|
NM_001289936.1:c.3645G>T , LRG_724t4:c.3645G>T
|
NP_001276865.1:p.Arg1215=
|
|
NM_001289937.1:c.*269G>T
|
NP_001276866.1:n.*269G>T
|
|
NM_004448.3:c.3690G>T , LRG_724t2:c.3690G>T
|
NP_004439.2:p.Arg1230=
|
|
NR_110535.1:n.4014G>T
|
|
|
XM_024450641.1:c.3828G>T
|
XP_024306409.1:p.Arg1276=
|
|
XM_024450642.1:c.3783G>T
|
XP_024306410.1:p.Arg1261=
|
|
XM_024450643.1:c.3738G>T
|
XP_024306411.1:p.Arg1246=
|
|
NM_001005862.3:c.3600G>T
|
NP_001005862.1:p.Arg1200=
|
|
NM_001289936.2:c.3645G>T
|
NP_001276865.1:p.Arg1215=
|
|
NM_001289937.2:c.*269G>T
|
NP_001276866.1:n.*269G>T
|
|
NM_001382782.1:c.3600G>T
|
NP_001369711.1:p.Arg1200=
|
|
NM_001382783.1:c.3600G>T
|
NP_001369712.1:p.Arg1200=
|
|
NM_001382784.1:c.3807G>T
|
NP_001369713.1:p.Arg1269=
|
|
NM_001382785.1:c.3792G>T
|
NP_001369714.1:p.Arg1264=
|
|
NM_001382786.1:c.3771G>T
|
NP_001369715.1:p.Arg1257=
|
|
NM_001382787.1:c.3765G>T
|
NP_001369716.1:p.Arg1255=
|
|
NM_001382788.1:c.3720G>T
|
NP_001369717.1:p.Arg1240=
|
|
NM_001382789.1:c.3711G>T
|
NP_001369718.1:p.Arg1237=
|
|
NM_001382790.1:c.3687G>T
|
NP_001369719.1:p.Arg1229=
|
|
NM_001382791.1:c.3681G>T
|
NP_001369720.1:p.Arg1227=
|
|
NM_001382792.1:c.3654G>T
|
NP_001369721.1:p.Arg1218=
|
|
NM_001382793.1:c.3648G>T
|
NP_001369722.1:p.Arg1216=
|
|
NM_001382794.1:c.3648G>T
|
NP_001369723.1:p.Arg1216=
|
|
NM_001382795.1:c.3642G>T
|
NP_001369724.1:p.Arg1214=
|
|
NM_001382796.1:c.3603G>T
|
NP_001369725.1:p.Arg1201=
|
|
NM_001382797.1:c.3591G>T
|
NP_001369726.1:p.Arg1197=
|
|
NM_001382798.1:c.3534G>T
|
NP_001369727.1:p.Arg1178=
|
|
NM_001382799.1:c.3510G>T
|
NP_001369728.1:p.Arg1170=
|
|
NM_001382800.1:c.3504G>T
|
NP_001369729.1:p.Arg1168=
|
|
NM_001382801.1:c.3486G>T
|
NP_001369730.1:p.Arg1162=
|
|
NM_001382802.1:c.3432G>T
|
NP_001369731.1:p.Arg1144=
|
|
NM_001382803.1:c.*269G>T
|
NP_001369732.1:n.*269G>T
|
|
NM_001382804.1:c.2862G>T
|
NP_001369733.1:p.Arg954=
|
|
NM_001382805.1:c.2739G>T
|
NP_001369734.1:p.Arg913=
|
|
NM_001382806.1:c.2652G>T
|
NP_001369735.1:p.Arg884=
|
|
NM_004448.4:c.3690G>T
MANE Select
|
NP_004439.2:p.Arg1230=
|
|
NR_110535.2:n.3928G>T
|
|
|