|
ENST00000269571.10:c.3256T>G
MANE Select
|
ENSP00000269571.4:p.Phe1086Val
|
|
|
ENST00000269571.9:c.3256T>G
|
ENSP00000269571.4:p.Phe1086Val
|
|
|
ENST00000406381.6:c.3166T>G
|
ENSP00000385185.2:p.Phe1056Val
|
|
|
ENST00000445658.6:c.2428T>G
|
ENSP00000404047.2:p.Phe810Val
|
|
|
ENST00000541774.5:c.3211T>G
|
ENSP00000446466.1:p.Phe1071Val
|
|
|
ENST00000578373.5:c.*3046T>G
|
ENSP00000463427.1:n.*3046T>G
|
|
|
ENST00000584450.5:c.3160-298T>G
|
ENSP00000463714.1:n.3160-298T>G
|
|
|
ENST00000584601.5:c.3166T>G
|
ENSP00000462438.1:p.Phe1056Val
|
|
|
NM_001005862.2:c.3166T>G , LRG_724t1:c.3166T>G
|
NP_001005862.1:p.Phe1056Val
|
|
|
NM_001289936.1:c.3211T>G , LRG_724t4:c.3211T>G
|
NP_001276865.1:p.Phe1071Val
|
|
|
NM_001289937.1:c.3160-298T>G
|
NP_001276866.1:n.3160-298T>G
|
|
|
NM_004448.3:c.3256T>G , LRG_724t2:c.3256T>G
|
NP_004439.2:p.Phe1086Val
|
|
|
NR_110535.1:n.3580T>G
|
|
|
|
XM_024450641.1:c.3394T>G
|
XP_024306409.1:p.Phe1132Val
|
|
|
XM_024450642.1:c.3349T>G
|
XP_024306410.1:p.Phe1117Val
|
|
|
XM_024450643.1:c.3304T>G
|
XP_024306411.1:p.Phe1102Val
|
|
|
NM_001005862.3:c.3166T>G
|
NP_001005862.1:p.Phe1056Val
|
|
|
NM_001289936.2:c.3211T>G
|
NP_001276865.1:p.Phe1071Val
|
|
|
NM_001289937.2:c.3160-298T>G
|
NP_001276866.1:n.3160-298T>G
|
|
|
NM_001382782.1:c.3166T>G
|
NP_001369711.1:p.Phe1056Val
|
|
|
NM_001382783.1:c.3166T>G
|
NP_001369712.1:p.Phe1056Val
|
|
|
NM_001382784.1:c.3373T>G
|
NP_001369713.1:p.Phe1125Val
|
|
|
NM_001382785.1:c.3358T>G
|
NP_001369714.1:p.Phe1120Val
|
|
|
NM_001382786.1:c.3337T>G
|
NP_001369715.1:p.Phe1113Val
|
|
|
NM_001382787.1:c.3331T>G
|
NP_001369716.1:p.Phe1111Val
|
|
|
NM_001382788.1:c.3286T>G
|
NP_001369717.1:p.Phe1096Val
|
|
|
NM_001382789.1:c.3277T>G
|
NP_001369718.1:p.Phe1093Val
|
|
|
NM_001382790.1:c.3253T>G
|
NP_001369719.1:p.Phe1085Val
|
|
|
NM_001382791.1:c.3247T>G
|
NP_001369720.1:p.Phe1083Val
|
|
|
NM_001382792.1:c.3220T>G
|
NP_001369721.1:p.Phe1074Val
|
|
|
NM_001382793.1:c.3214T>G
|
NP_001369722.1:p.Phe1072Val
|
|
|
NM_001382794.1:c.3214T>G
|
NP_001369723.1:p.Phe1072Val
|
|
|
NM_001382795.1:c.3208T>G
|
NP_001369724.1:p.Phe1070Val
|
|
|
NM_001382796.1:c.3169T>G
|
NP_001369725.1:p.Phe1057Val
|
|
|
NM_001382797.1:c.3157T>G
|
NP_001369726.1:p.Phe1053Val
|
|
|
NM_001382798.1:c.3100T>G
|
NP_001369727.1:p.Phe1034Val
|
|
|
NM_001382799.1:c.3076T>G
|
NP_001369728.1:p.Phe1026Val
|
|
|
NM_001382800.1:c.3070T>G
|
NP_001369729.1:p.Phe1024Val
|
|
|
NM_001382801.1:c.3052T>G
|
NP_001369730.1:p.Phe1018Val
|
|
|
NM_001382802.1:c.2998T>G
|
NP_001369731.1:p.Phe1000Val
|
|
|
NM_001382803.1:c.3118-298T>G
|
NP_001369732.1:n.3118-298T>G
|
|
|
NM_001382804.1:c.2428T>G
|
NP_001369733.1:p.Phe810Val
|
|
|
NM_001382805.1:c.2305T>G
|
NP_001369734.1:p.Phe769Val
|
|
|
NM_001382806.1:c.2218T>G
|
NP_001369735.1:p.Phe740Val
|
|
|
NM_004448.4:c.3256T>G
MANE Select
|
NP_004439.2:p.Phe1086Val
|
|
|
NR_110535.2:n.3494T>G
|
|
|
