|
ENST00000269571.10:c.2518C>G
MANE Select
|
ENSP00000269571.4:p.Arg840Gly
|
|
|
ENST00000269571.9:c.2518C>G
|
ENSP00000269571.4:p.Arg840Gly
|
|
|
ENST00000406381.6:c.2428C>G
|
ENSP00000385185.2:p.Arg810Gly
|
|
|
ENST00000445658.6:c.1690C>G
|
ENSP00000404047.2:p.Arg564Gly
|
|
|
ENST00000541774.5:c.2473C>G
|
ENSP00000446466.1:p.Arg825Gly
|
|
|
ENST00000578373.5:c.*2308C>G
|
ENSP00000463427.1:n.*2308C>G
|
|
|
ENST00000580074.1:c.624C>G
|
|
|
|
ENST00000583038.5:n.3652C>G
|
|
|
|
ENST00000584450.5:c.2518C>G
|
ENSP00000463714.1:p.Arg840Gly
|
|
|
ENST00000584601.5:c.2428C>G
|
ENSP00000462438.1:p.Arg810Gly
|
|
|
NM_001005862.2:c.2428C>G , LRG_724t1:c.2428C>G
|
NP_001005862.1:p.Arg810Gly
|
|
|
NM_001289936.1:c.2473C>G , LRG_724t4:c.2473C>G
|
NP_001276865.1:p.Arg825Gly
|
|
|
NM_001289937.1:c.2518C>G
|
NP_001276866.1:p.Arg840Gly
|
|
|
NM_004448.3:c.2518C>G , LRG_724t2:c.2518C>G
|
NP_004439.2:p.Arg840Gly
|
|
|
NR_110535.1:n.2842C>G
|
|
|
|
XM_024450641.1:c.2656C>G
|
XP_024306409.1:p.Arg886Gly
|
|
|
XM_024450642.1:c.2611C>G
|
XP_024306410.1:p.Arg871Gly
|
|
|
XM_024450643.1:c.2566C>G
|
XP_024306411.1:p.Arg856Gly
|
|
|
NM_001005862.3:c.2428C>G
|
NP_001005862.1:p.Arg810Gly
|
|
|
NM_001289936.2:c.2473C>G
|
NP_001276865.1:p.Arg825Gly
|
|
|
NM_001289937.2:c.2518C>G
|
NP_001276866.1:p.Arg840Gly
|
|
|
NM_001382782.1:c.2428C>G
|
NP_001369711.1:p.Arg810Gly
|
|
|
NM_001382783.1:c.2428C>G
|
NP_001369712.1:p.Arg810Gly
|
|
|
NM_001382784.1:c.2635C>G
|
NP_001369713.1:p.Arg879Gly
|
|
|
NM_001382785.1:c.2620C>G
|
NP_001369714.1:p.Arg874Gly
|
|
|
NM_001382786.1:c.2599C>G
|
NP_001369715.1:p.Arg867Gly
|
|
|
NM_001382787.1:c.2593C>G
|
NP_001369716.1:p.Arg865Gly
|
|
|
NM_001382788.1:c.2548C>G
|
NP_001369717.1:p.Arg850Gly
|
|
|
NM_001382789.1:c.2539C>G
|
NP_001369718.1:p.Arg847Gly
|
|
|
NM_001382790.1:c.2515C>G
|
NP_001369719.1:p.Arg839Gly
|
|
|
NM_001382791.1:c.2509C>G
|
NP_001369720.1:p.Arg837Gly
|
|
|
NM_001382792.1:c.2482C>G
|
NP_001369721.1:p.Arg828Gly
|
|
|
NM_001382793.1:c.2476C>G
|
NP_001369722.1:p.Arg826Gly
|
|
|
NM_001382794.1:c.2476C>G
|
NP_001369723.1:p.Arg826Gly
|
|
|
NM_001382795.1:c.2470C>G
|
NP_001369724.1:p.Arg824Gly
|
|
|
NM_001382796.1:c.2518C>G
|
NP_001369725.1:p.Arg840Gly
|
|
|
NM_001382797.1:c.2419C>G
|
NP_001369726.1:p.Arg807Gly
|
|
|
NM_001382798.1:c.2493+162C>G
|
NP_001369727.1:n.2493+162C>G
|
|
|
NM_001382799.1:c.2338C>G
|
NP_001369728.1:p.Arg780Gly
|
|
|
NM_001382800.1:c.2332C>G
|
NP_001369729.1:p.Arg778Gly
|
|
|
NM_001382801.1:c.2445+162C>G
|
NP_001369730.1:n.2445+162C>G
|
|
|
NM_001382802.1:c.2260C>G
|
NP_001369731.1:p.Arg754Gly
|
|
|
NM_001382803.1:c.2476C>G
|
NP_001369732.1:p.Arg826Gly
|
|
|
NM_001382804.1:c.1690C>G
|
NP_001369733.1:p.Arg564Gly
|
|
|
NM_001382805.1:c.2208+1413C>G
|
NP_001369734.1:n.2208+1413C>G
|
|
|
NM_001382806.1:c.1480C>G
|
NP_001369735.1:p.Arg494Gly
|
|
|
NM_004448.4:c.2518C>G
MANE Select
|
NP_004439.2:p.Arg840Gly
|
|
|
NR_110535.2:n.2756C>G
|
|
|
