ENST00000269571.10:c.3649T>G
MANE Select
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ENSP00000269571.4:p.Phe1217Val
|
|
ENST00000269571.9:c.3649T>G
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ENSP00000269571.4:p.Phe1217Val
|
|
ENST00000406381.6:c.3559T>G
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ENSP00000385185.2:p.Phe1187Val
|
|
ENST00000445658.6:c.2821T>G
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ENSP00000404047.2:p.Phe941Val
|
|
ENST00000541774.5:c.3604T>G
|
ENSP00000446466.1:p.Phe1202Val
|
|
ENST00000578373.5:c.*3439T>G
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ENSP00000463427.1:n.*3439T>G
|
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ENST00000584450.5:c.*228T>G
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ENSP00000463714.1:n.*228T>G
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ENST00000584601.5:c.3559T>G
|
ENSP00000462438.1:p.Phe1187Val
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NM_001005862.2:c.3559T>G , LRG_724t1:c.3559T>G
|
NP_001005862.1:p.Phe1187Val
|
|
NM_001289936.1:c.3604T>G , LRG_724t4:c.3604T>G
|
NP_001276865.1:p.Phe1202Val
|
|
NM_001289937.1:c.*228T>G
|
NP_001276866.1:n.*228T>G
|
|
NM_004448.3:c.3649T>G , LRG_724t2:c.3649T>G
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NP_004439.2:p.Phe1217Val
|
|
NR_110535.1:n.3973T>G
|
|
|
XM_024450641.1:c.3787T>G
|
XP_024306409.1:p.Phe1263Val
|
|
XM_024450642.1:c.3742T>G
|
XP_024306410.1:p.Phe1248Val
|
|
XM_024450643.1:c.3697T>G
|
XP_024306411.1:p.Phe1233Val
|
|
NM_001005862.3:c.3559T>G
|
NP_001005862.1:p.Phe1187Val
|
|
NM_001289936.2:c.3604T>G
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NP_001276865.1:p.Phe1202Val
|
|
NM_001289937.2:c.*228T>G
|
NP_001276866.1:n.*228T>G
|
|
NM_001382782.1:c.3559T>G
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NP_001369711.1:p.Phe1187Val
|
|
NM_001382783.1:c.3559T>G
|
NP_001369712.1:p.Phe1187Val
|
|
NM_001382784.1:c.3766T>G
|
NP_001369713.1:p.Phe1256Val
|
|
NM_001382785.1:c.3751T>G
|
NP_001369714.1:p.Phe1251Val
|
|
NM_001382786.1:c.3730T>G
|
NP_001369715.1:p.Phe1244Val
|
|
NM_001382787.1:c.3724T>G
|
NP_001369716.1:p.Phe1242Val
|
|
NM_001382788.1:c.3679T>G
|
NP_001369717.1:p.Phe1227Val
|
|
NM_001382789.1:c.3670T>G
|
NP_001369718.1:p.Phe1224Val
|
|
NM_001382790.1:c.3646T>G
|
NP_001369719.1:p.Phe1216Val
|
|
NM_001382791.1:c.3640T>G
|
NP_001369720.1:p.Phe1214Val
|
|
NM_001382792.1:c.3613T>G
|
NP_001369721.1:p.Phe1205Val
|
|
NM_001382793.1:c.3607T>G
|
NP_001369722.1:p.Phe1203Val
|
|
NM_001382794.1:c.3607T>G
|
NP_001369723.1:p.Phe1203Val
|
|
NM_001382795.1:c.3601T>G
|
NP_001369724.1:p.Phe1201Val
|
|
NM_001382796.1:c.3562T>G
|
NP_001369725.1:p.Phe1188Val
|
|
NM_001382797.1:c.3550T>G
|
NP_001369726.1:p.Phe1184Val
|
|
NM_001382798.1:c.3493T>G
|
NP_001369727.1:p.Phe1165Val
|
|
NM_001382799.1:c.3469T>G
|
NP_001369728.1:p.Phe1157Val
|
|
NM_001382800.1:c.3463T>G
|
NP_001369729.1:p.Phe1155Val
|
|
NM_001382801.1:c.3445T>G
|
NP_001369730.1:p.Phe1149Val
|
|
NM_001382802.1:c.3391T>G
|
NP_001369731.1:p.Phe1131Val
|
|
NM_001382803.1:c.*228T>G
|
NP_001369732.1:n.*228T>G
|
|
NM_001382804.1:c.2821T>G
|
NP_001369733.1:p.Phe941Val
|
|
NM_001382805.1:c.2698T>G
|
NP_001369734.1:p.Phe900Val
|
|
NM_001382806.1:c.2611T>G
|
NP_001369735.1:p.Phe871Val
|
|
NM_004448.4:c.3649T>G
MANE Select
|
NP_004439.2:p.Phe1217Val
|
|
NR_110535.2:n.3887T>G
|
|
|