ENST00000269571.10:c.2532G>C
MANE Select
|
ENSP00000269571.4:p.Arg844Ser
|
|
ENST00000269571.9:c.2532G>C
|
ENSP00000269571.4:p.Arg844Ser
|
|
ENST00000406381.6:c.2442G>C
|
ENSP00000385185.2:p.Arg814Ser
|
|
ENST00000445658.6:c.1704G>C
|
ENSP00000404047.2:p.Arg568Ser
|
|
ENST00000541774.5:c.2487G>C
|
ENSP00000446466.1:p.Arg829Ser
|
|
ENST00000578373.5:c.*2322G>C
|
ENSP00000463427.1:n.*2322G>C
|
|
ENST00000580074.1:c.638G>C
|
|
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ENST00000583038.5:n.3666G>C
|
|
|
ENST00000584450.5:c.2532G>C
|
ENSP00000463714.1:p.Arg844Ser
|
|
ENST00000584601.5:c.2442G>C
|
ENSP00000462438.1:p.Arg814Ser
|
|
NM_001005862.2:c.2442G>C , LRG_724t1:c.2442G>C
|
NP_001005862.1:p.Arg814Ser
|
|
NM_001289936.1:c.2487G>C , LRG_724t4:c.2487G>C
|
NP_001276865.1:p.Arg829Ser
|
|
NM_001289937.1:c.2532G>C
|
NP_001276866.1:p.Arg844Ser
|
|
NM_004448.3:c.2532G>C , LRG_724t2:c.2532G>C
|
NP_004439.2:p.Arg844Ser
|
|
NR_110535.1:n.2856G>C
|
|
|
XM_024450641.1:c.2670G>C
|
XP_024306409.1:p.Arg890Ser
|
|
XM_024450642.1:c.2625G>C
|
XP_024306410.1:p.Arg875Ser
|
|
XM_024450643.1:c.2580G>C
|
XP_024306411.1:p.Arg860Ser
|
|
NM_001005862.3:c.2442G>C
|
NP_001005862.1:p.Arg814Ser
|
|
NM_001289936.2:c.2487G>C
|
NP_001276865.1:p.Arg829Ser
|
|
NM_001289937.2:c.2532G>C
|
NP_001276866.1:p.Arg844Ser
|
|
NM_001382782.1:c.2442G>C
|
NP_001369711.1:p.Arg814Ser
|
|
NM_001382783.1:c.2442G>C
|
NP_001369712.1:p.Arg814Ser
|
|
NM_001382784.1:c.2649G>C
|
NP_001369713.1:p.Arg883Ser
|
|
NM_001382785.1:c.2634G>C
|
NP_001369714.1:p.Arg878Ser
|
|
NM_001382786.1:c.2613G>C
|
NP_001369715.1:p.Arg871Ser
|
|
NM_001382787.1:c.2607G>C
|
NP_001369716.1:p.Arg869Ser
|
|
NM_001382788.1:c.2562G>C
|
NP_001369717.1:p.Arg854Ser
|
|
NM_001382789.1:c.2553G>C
|
NP_001369718.1:p.Arg851Ser
|
|
NM_001382790.1:c.2529G>C
|
NP_001369719.1:p.Arg843Ser
|
|
NM_001382791.1:c.2523G>C
|
NP_001369720.1:p.Arg841Ser
|
|
NM_001382792.1:c.2496G>C
|
NP_001369721.1:p.Arg832Ser
|
|
NM_001382793.1:c.2490G>C
|
NP_001369722.1:p.Arg830Ser
|
|
NM_001382794.1:c.2490G>C
|
NP_001369723.1:p.Arg830Ser
|
|
NM_001382795.1:c.2484G>C
|
NP_001369724.1:p.Arg828Ser
|
|
NM_001382796.1:c.2532G>C
|
NP_001369725.1:p.Arg844Ser
|
|
NM_001382797.1:c.2433G>C
|
NP_001369726.1:p.Arg811Ser
|
|
NM_001382798.1:c.2493+176G>C
|
NP_001369727.1:n.2493+176G>C
|
|
NM_001382799.1:c.2352G>C
|
NP_001369728.1:p.Arg784Ser
|
|
NM_001382800.1:c.2346G>C
|
NP_001369729.1:p.Arg782Ser
|
|
NM_001382801.1:c.2445+176G>C
|
NP_001369730.1:n.2445+176G>C
|
|
NM_001382802.1:c.2274G>C
|
NP_001369731.1:p.Arg758Ser
|
|
NM_001382803.1:c.2490G>C
|
NP_001369732.1:p.Arg830Ser
|
|
NM_001382804.1:c.1704G>C
|
NP_001369733.1:p.Arg568Ser
|
|
NM_001382805.1:c.2208+1427G>C
|
NP_001369734.1:n.2208+1427G>C
|
|
NM_001382806.1:c.1494G>C
|
NP_001369735.1:p.Arg498Ser
|
|
NM_004448.4:c.2532G>C
MANE Select
|
NP_004439.2:p.Arg844Ser
|
|
NR_110535.2:n.2770G>C
|
|
|