|
ENST00000269571.10:c.3553T>G
MANE Select
|
ENSP00000269571.4:p.Phe1185Val
|
|
|
ENST00000269571.9:c.3553T>G
|
ENSP00000269571.4:p.Phe1185Val
|
|
|
ENST00000406381.6:c.3463T>G
|
ENSP00000385185.2:p.Phe1155Val
|
|
|
ENST00000445658.6:c.2725T>G
|
ENSP00000404047.2:p.Phe909Val
|
|
|
ENST00000541774.5:c.3508T>G
|
ENSP00000446466.1:p.Phe1170Val
|
|
|
ENST00000578373.5:c.*3343T>G
|
ENSP00000463427.1:n.*3343T>G
|
|
|
ENST00000584450.5:c.*132T>G
|
ENSP00000463714.1:n.*132T>G
|
|
|
ENST00000584601.5:c.3463T>G
|
ENSP00000462438.1:p.Phe1155Val
|
|
|
NM_001005862.2:c.3463T>G , LRG_724t1:c.3463T>G
|
NP_001005862.1:p.Phe1155Val
|
|
|
NM_001289936.1:c.3508T>G , LRG_724t4:c.3508T>G
|
NP_001276865.1:p.Phe1170Val
|
|
|
NM_001289937.1:c.*132T>G
|
NP_001276866.1:n.*132T>G
|
|
|
NM_004448.3:c.3553T>G , LRG_724t2:c.3553T>G
|
NP_004439.2:p.Phe1185Val
|
|
|
NR_110535.1:n.3877T>G
|
|
|
|
XM_024450641.1:c.3691T>G
|
XP_024306409.1:p.Phe1231Val
|
|
|
XM_024450642.1:c.3646T>G
|
XP_024306410.1:p.Phe1216Val
|
|
|
XM_024450643.1:c.3601T>G
|
XP_024306411.1:p.Phe1201Val
|
|
|
NM_001005862.3:c.3463T>G
|
NP_001005862.1:p.Phe1155Val
|
|
|
NM_001289936.2:c.3508T>G
|
NP_001276865.1:p.Phe1170Val
|
|
|
NM_001289937.2:c.*132T>G
|
NP_001276866.1:n.*132T>G
|
|
|
NM_001382782.1:c.3463T>G
|
NP_001369711.1:p.Phe1155Val
|
|
|
NM_001382783.1:c.3463T>G
|
NP_001369712.1:p.Phe1155Val
|
|
|
NM_001382784.1:c.3670T>G
|
NP_001369713.1:p.Phe1224Val
|
|
|
NM_001382785.1:c.3655T>G
|
NP_001369714.1:p.Phe1219Val
|
|
|
NM_001382786.1:c.3634T>G
|
NP_001369715.1:p.Phe1212Val
|
|
|
NM_001382787.1:c.3628T>G
|
NP_001369716.1:p.Phe1210Val
|
|
|
NM_001382788.1:c.3583T>G
|
NP_001369717.1:p.Phe1195Val
|
|
|
NM_001382789.1:c.3574T>G
|
NP_001369718.1:p.Phe1192Val
|
|
|
NM_001382790.1:c.3550T>G
|
NP_001369719.1:p.Phe1184Val
|
|
|
NM_001382791.1:c.3544T>G
|
NP_001369720.1:p.Phe1182Val
|
|
|
NM_001382792.1:c.3517T>G
|
NP_001369721.1:p.Phe1173Val
|
|
|
NM_001382793.1:c.3511T>G
|
NP_001369722.1:p.Phe1171Val
|
|
|
NM_001382794.1:c.3511T>G
|
NP_001369723.1:p.Phe1171Val
|
|
|
NM_001382795.1:c.3505T>G
|
NP_001369724.1:p.Phe1169Val
|
|
|
NM_001382796.1:c.3466T>G
|
NP_001369725.1:p.Phe1156Val
|
|
|
NM_001382797.1:c.3454T>G
|
NP_001369726.1:p.Phe1152Val
|
|
|
NM_001382798.1:c.3397T>G
|
NP_001369727.1:p.Phe1133Val
|
|
|
NM_001382799.1:c.3373T>G
|
NP_001369728.1:p.Phe1125Val
|
|
|
NM_001382800.1:c.3367T>G
|
NP_001369729.1:p.Phe1123Val
|
|
|
NM_001382801.1:c.3349T>G
|
NP_001369730.1:p.Phe1117Val
|
|
|
NM_001382802.1:c.3295T>G
|
NP_001369731.1:p.Phe1099Val
|
|
|
NM_001382803.1:c.*132T>G
|
NP_001369732.1:n.*132T>G
|
|
|
NM_001382804.1:c.2725T>G
|
NP_001369733.1:p.Phe909Val
|
|
|
NM_001382805.1:c.2602T>G
|
NP_001369734.1:p.Phe868Val
|
|
|
NM_001382806.1:c.2515T>G
|
NP_001369735.1:p.Phe839Val
|
|
|
NM_004448.4:c.3553T>G
MANE Select
|
NP_004439.2:p.Phe1185Val
|
|
|
NR_110535.2:n.3791T>G
|
|
|
