ENST00000269571.10:c.2516T>C
MANE Select
|
ENSP00000269571.4:p.Val839Ala
|
|
ENST00000269571.9:c.2516T>C
|
ENSP00000269571.4:p.Val839Ala
|
|
ENST00000406381.6:c.2426T>C
|
ENSP00000385185.2:p.Val809Ala
|
|
ENST00000445658.6:c.1688T>C
|
ENSP00000404047.2:p.Val563Ala
|
|
ENST00000541774.5:c.2471T>C
|
ENSP00000446466.1:p.Val824Ala
|
|
ENST00000578373.5:c.*2306T>C
|
ENSP00000463427.1:n.*2306T>C
|
|
ENST00000580074.1:c.622T>C
|
|
|
ENST00000583038.5:n.3650T>C
|
|
|
ENST00000584450.5:c.2516T>C
|
ENSP00000463714.1:p.Val839Ala
|
|
ENST00000584601.5:c.2426T>C
|
ENSP00000462438.1:p.Val809Ala
|
|
NM_001005862.2:c.2426T>C , LRG_724t1:c.2426T>C
|
NP_001005862.1:p.Val809Ala
|
|
NM_001289936.1:c.2471T>C , LRG_724t4:c.2471T>C
|
NP_001276865.1:p.Val824Ala
|
|
NM_001289937.1:c.2516T>C
|
NP_001276866.1:p.Val839Ala
|
|
NM_004448.3:c.2516T>C , LRG_724t2:c.2516T>C
|
NP_004439.2:p.Val839Ala
|
|
NR_110535.1:n.2840T>C
|
|
|
XM_024450641.1:c.2654T>C
|
XP_024306409.1:p.Val885Ala
|
|
XM_024450642.1:c.2609T>C
|
XP_024306410.1:p.Val870Ala
|
|
XM_024450643.1:c.2564T>C
|
XP_024306411.1:p.Val855Ala
|
|
NM_001005862.3:c.2426T>C
|
NP_001005862.1:p.Val809Ala
|
|
NM_001289936.2:c.2471T>C
|
NP_001276865.1:p.Val824Ala
|
|
NM_001289937.2:c.2516T>C
|
NP_001276866.1:p.Val839Ala
|
|
NM_001382782.1:c.2426T>C
|
NP_001369711.1:p.Val809Ala
|
|
NM_001382783.1:c.2426T>C
|
NP_001369712.1:p.Val809Ala
|
|
NM_001382784.1:c.2633T>C
|
NP_001369713.1:p.Val878Ala
|
|
NM_001382785.1:c.2618T>C
|
NP_001369714.1:p.Val873Ala
|
|
NM_001382786.1:c.2597T>C
|
NP_001369715.1:p.Val866Ala
|
|
NM_001382787.1:c.2591T>C
|
NP_001369716.1:p.Val864Ala
|
|
NM_001382788.1:c.2546T>C
|
NP_001369717.1:p.Val849Ala
|
|
NM_001382789.1:c.2537T>C
|
NP_001369718.1:p.Val846Ala
|
|
NM_001382790.1:c.2513T>C
|
NP_001369719.1:p.Val838Ala
|
|
NM_001382791.1:c.2507T>C
|
NP_001369720.1:p.Val836Ala
|
|
NM_001382792.1:c.2480T>C
|
NP_001369721.1:p.Val827Ala
|
|
NM_001382793.1:c.2474T>C
|
NP_001369722.1:p.Val825Ala
|
|
NM_001382794.1:c.2474T>C
|
NP_001369723.1:p.Val825Ala
|
|
NM_001382795.1:c.2468T>C
|
NP_001369724.1:p.Val823Ala
|
|
NM_001382796.1:c.2516T>C
|
NP_001369725.1:p.Val839Ala
|
|
NM_001382797.1:c.2417T>C
|
NP_001369726.1:p.Val806Ala
|
|
NM_001382798.1:c.2493+160T>C
|
NP_001369727.1:n.2493+160T>C
|
|
NM_001382799.1:c.2336T>C
|
NP_001369728.1:p.Val779Ala
|
|
NM_001382800.1:c.2330T>C
|
NP_001369729.1:p.Val777Ala
|
|
NM_001382801.1:c.2445+160T>C
|
NP_001369730.1:n.2445+160T>C
|
|
NM_001382802.1:c.2258T>C
|
NP_001369731.1:p.Val753Ala
|
|
NM_001382803.1:c.2474T>C
|
NP_001369732.1:p.Val825Ala
|
|
NM_001382804.1:c.1688T>C
|
NP_001369733.1:p.Val563Ala
|
|
NM_001382805.1:c.2208+1411T>C
|
NP_001369734.1:n.2208+1411T>C
|
|
NM_001382806.1:c.1478T>C
|
NP_001369735.1:p.Val493Ala
|
|
NM_004448.4:c.2516T>C
MANE Select
|
NP_004439.2:p.Val839Ala
|
|
NR_110535.2:n.2754T>C
|
|
|