|
ENST00000269571.10:c.2375C>G
MANE Select
|
ENSP00000269571.4:p.Ser792Cys
|
|
|
ENST00000269571.9:c.2375C>G
|
ENSP00000269571.4:p.Ser792Cys
|
|
|
ENST00000406381.6:c.2285C>G
|
ENSP00000385185.2:p.Ser762Cys
|
|
|
ENST00000445658.6:c.1547C>G
|
ENSP00000404047.2:p.Ser516Cys
|
|
|
ENST00000541774.5:c.2330C>G
|
ENSP00000446466.1:p.Ser777Cys
|
|
|
ENST00000578373.5:c.*2165C>G
|
ENSP00000463427.1:n.*2165C>G
|
|
|
ENST00000580074.1:c.481C>G
|
|
|
|
ENST00000583038.5:n.3509C>G
|
|
|
|
ENST00000584450.5:c.2375C>G
|
ENSP00000463714.1:p.Ser792Cys
|
|
|
ENST00000584601.5:c.2285C>G
|
ENSP00000462438.1:p.Ser762Cys
|
|
|
NM_001005862.2:c.2285C>G , LRG_724t1:c.2285C>G
|
NP_001005862.1:p.Ser762Cys
|
|
|
NM_001289936.1:c.2330C>G , LRG_724t4:c.2330C>G
|
NP_001276865.1:p.Ser777Cys
|
|
|
NM_001289937.1:c.2375C>G
|
NP_001276866.1:p.Ser792Cys
|
|
|
NM_004448.3:c.2375C>G , LRG_724t2:c.2375C>G
|
NP_004439.2:p.Ser792Cys
|
|
|
NR_110535.1:n.2699C>G
|
|
|
|
XM_024450641.1:c.2513C>G
|
XP_024306409.1:p.Ser838Cys
|
|
|
XM_024450642.1:c.2468C>G
|
XP_024306410.1:p.Ser823Cys
|
|
|
XM_024450643.1:c.2423C>G
|
XP_024306411.1:p.Ser808Cys
|
|
|
NM_001005862.3:c.2285C>G
|
NP_001005862.1:p.Ser762Cys
|
|
|
NM_001289936.2:c.2330C>G
|
NP_001276865.1:p.Ser777Cys
|
|
|
NM_001289937.2:c.2375C>G
|
NP_001276866.1:p.Ser792Cys
|
|
|
NM_001382782.1:c.2285C>G
|
NP_001369711.1:p.Ser762Cys
|
|
|
NM_001382783.1:c.2285C>G
|
NP_001369712.1:p.Ser762Cys
|
|
|
NM_001382784.1:c.2492C>G
|
NP_001369713.1:p.Ser831Cys
|
|
|
NM_001382785.1:c.2477C>G
|
NP_001369714.1:p.Ser826Cys
|
|
|
NM_001382786.1:c.2456C>G
|
NP_001369715.1:p.Ser819Cys
|
|
|
NM_001382787.1:c.2450C>G
|
NP_001369716.1:p.Ser817Cys
|
|
|
NM_001382788.1:c.2405C>G
|
NP_001369717.1:p.Ser802Cys
|
|
|
NM_001382789.1:c.2396C>G
|
NP_001369718.1:p.Ser799Cys
|
|
|
NM_001382790.1:c.2372C>G
|
NP_001369719.1:p.Ser791Cys
|
|
|
NM_001382791.1:c.2366C>G
|
NP_001369720.1:p.Ser789Cys
|
|
|
NM_001382792.1:c.2339C>G
|
NP_001369721.1:p.Ser780Cys
|
|
|
NM_001382793.1:c.2333C>G
|
NP_001369722.1:p.Ser778Cys
|
|
|
NM_001382794.1:c.2333C>G
|
NP_001369723.1:p.Ser778Cys
|
|
|
NM_001382795.1:c.2327C>G
|
NP_001369724.1:p.Ser776Cys
|
|
|
NM_001382796.1:c.2375C>G
|
NP_001369725.1:p.Ser792Cys
|
|
|
NM_001382797.1:c.2276C>G
|
NP_001369726.1:p.Ser759Cys
|
|
|
NM_001382798.1:c.2375C>G
|
NP_001369727.1:p.Ser792Cys
|
|
|
NM_001382799.1:c.2195C>G
|
NP_001369728.1:p.Ser732Cys
|
|
|
NM_001382800.1:c.2308-256C>G
|
NP_001369729.1:n.2308-256C>G
|
|
|
NM_001382801.1:c.2327C>G
|
NP_001369730.1:p.Ser776Cys
|
|
|
NM_001382802.1:c.2117C>G
|
NP_001369731.1:p.Ser706Cys
|
|
|
NM_001382803.1:c.2333C>G
|
NP_001369732.1:p.Ser778Cys
|
|
|
NM_001382804.1:c.1547C>G
|
NP_001369733.1:p.Ser516Cys
|
|
|
NM_001382805.1:c.2208+1133C>G
|
NP_001369734.1:n.2208+1133C>G
|
|
|
NM_001382806.1:c.1337C>G
|
NP_001369735.1:p.Ser446Cys
|
|
|
NM_004448.4:c.2375C>G
MANE Select
|
NP_004439.2:p.Ser792Cys
|
|
|
NR_110535.2:n.2613C>G
|
|
|
