ENST00000269571.10:c.2320A>G
MANE Select
|
ENSP00000269571.4:p.Met774Val
|
|
ENST00000269571.9:c.2320A>G
|
ENSP00000269571.4:p.Met774Val
|
|
ENST00000406381.6:c.2230A>G
|
ENSP00000385185.2:p.Met744Val
|
|
ENST00000445658.6:c.1492A>G
|
ENSP00000404047.2:p.Met498Val
|
|
ENST00000541774.5:c.2275A>G
|
ENSP00000446466.1:p.Met759Val
|
|
ENST00000578373.5:c.*2110A>G
|
ENSP00000463427.1:n.*2110A>G
|
|
ENST00000580074.1:c.426A>G
|
|
|
ENST00000583038.5:n.3454A>G
|
|
|
ENST00000584450.5:c.2320A>G
|
ENSP00000463714.1:p.Met774Val
|
|
ENST00000584601.5:c.2230A>G
|
ENSP00000462438.1:p.Met744Val
|
|
NM_001005862.2:c.2230A>G , LRG_724t1:c.2230A>G
|
NP_001005862.1:p.Met744Val
|
|
NM_001289936.1:c.2275A>G , LRG_724t4:c.2275A>G
|
NP_001276865.1:p.Met759Val
|
|
NM_001289937.1:c.2320A>G
|
NP_001276866.1:p.Met774Val
|
|
NM_004448.3:c.2320A>G , LRG_724t2:c.2320A>G
|
NP_004439.2:p.Met774Val
|
|
NR_110535.1:n.2644A>G
|
|
|
XM_024450641.1:c.2458A>G
|
XP_024306409.1:p.Met820Val
|
|
XM_024450642.1:c.2413A>G
|
XP_024306410.1:p.Met805Val
|
|
XM_024450643.1:c.2368A>G
|
XP_024306411.1:p.Met790Val
|
|
NM_001005862.3:c.2230A>G
|
NP_001005862.1:p.Met744Val
|
|
NM_001289936.2:c.2275A>G
|
NP_001276865.1:p.Met759Val
|
|
NM_001289937.2:c.2320A>G
|
NP_001276866.1:p.Met774Val
|
|
NM_001382782.1:c.2230A>G
|
NP_001369711.1:p.Met744Val
|
|
NM_001382783.1:c.2230A>G
|
NP_001369712.1:p.Met744Val
|
|
NM_001382784.1:c.2437A>G
|
NP_001369713.1:p.Met813Val
|
|
NM_001382785.1:c.2422A>G
|
NP_001369714.1:p.Met808Val
|
|
NM_001382786.1:c.2401A>G
|
NP_001369715.1:p.Met801Val
|
|
NM_001382787.1:c.2395A>G
|
NP_001369716.1:p.Met799Val
|
|
NM_001382788.1:c.2350A>G
|
NP_001369717.1:p.Met784Val
|
|
NM_001382789.1:c.2341A>G
|
NP_001369718.1:p.Met781Val
|
|
NM_001382790.1:c.2317A>G
|
NP_001369719.1:p.Met773Val
|
|
NM_001382791.1:c.2311A>G
|
NP_001369720.1:p.Met771Val
|
|
NM_001382792.1:c.2284A>G
|
NP_001369721.1:p.Met762Val
|
|
NM_001382793.1:c.2278A>G
|
NP_001369722.1:p.Met760Val
|
|
NM_001382794.1:c.2278A>G
|
NP_001369723.1:p.Met760Val
|
|
NM_001382795.1:c.2272A>G
|
NP_001369724.1:p.Met758Val
|
|
NM_001382796.1:c.2320A>G
|
NP_001369725.1:p.Met774Val
|
|
NM_001382797.1:c.2221A>G
|
NP_001369726.1:p.Met741Val
|
|
NM_001382798.1:c.2320A>G
|
NP_001369727.1:p.Met774Val
|
|
NM_001382799.1:c.2140A>G
|
NP_001369728.1:p.Met714Val
|
|
NM_001382800.1:c.2308-311A>G
|
NP_001369729.1:n.2308-311A>G
|
|
NM_001382801.1:c.2272A>G
|
NP_001369730.1:p.Met758Val
|
|
NM_001382802.1:c.2062A>G
|
NP_001369731.1:p.Met688Val
|
|
NM_001382803.1:c.2278A>G
|
NP_001369732.1:p.Met760Val
|
|
NM_001382804.1:c.1492A>G
|
NP_001369733.1:p.Met498Val
|
|
NM_001382805.1:c.2208+1078A>G
|
NP_001369734.1:n.2208+1078A>G
|
|
NM_001382806.1:c.1282A>G
|
NP_001369735.1:p.Met428Val
|
|
NM_004448.4:c.2320A>G
MANE Select
|
NP_004439.2:p.Met774Val
|
|
NR_110535.2:n.2558A>G
|
|
|