ENST00000269571.10:c.2379G>C
MANE Select
|
ENSP00000269571.4:p.Thr793=
|
|
ENST00000269571.9:c.2379G>C
|
ENSP00000269571.4:p.Thr793=
|
|
ENST00000406381.6:c.2289G>C
|
ENSP00000385185.2:p.Thr763=
|
|
ENST00000445658.6:c.1551G>C
|
ENSP00000404047.2:p.Thr517=
|
|
ENST00000541774.5:c.2334G>C
|
ENSP00000446466.1:p.Thr778=
|
|
ENST00000578373.5:c.*2169G>C
|
ENSP00000463427.1:n.*2169G>C
|
|
ENST00000580074.1:c.485G>C
|
|
|
ENST00000583038.5:n.3513G>C
|
|
|
ENST00000584450.5:c.2379G>C
|
ENSP00000463714.1:p.Thr793=
|
|
ENST00000584601.5:c.2289G>C
|
ENSP00000462438.1:p.Thr763=
|
|
NM_001005862.2:c.2289G>C , LRG_724t1:c.2289G>C
|
NP_001005862.1:p.Thr763=
|
|
NM_001289936.1:c.2334G>C , LRG_724t4:c.2334G>C
|
NP_001276865.1:p.Thr778=
|
|
NM_001289937.1:c.2379G>C
|
NP_001276866.1:p.Thr793=
|
|
NM_004448.3:c.2379G>C , LRG_724t2:c.2379G>C
|
NP_004439.2:p.Thr793=
|
|
NR_110535.1:n.2703G>C
|
|
|
XM_024450641.1:c.2517G>C
|
XP_024306409.1:p.Thr839=
|
|
XM_024450642.1:c.2472G>C
|
XP_024306410.1:p.Thr824=
|
|
XM_024450643.1:c.2427G>C
|
XP_024306411.1:p.Thr809=
|
|
NM_001005862.3:c.2289G>C
|
NP_001005862.1:p.Thr763=
|
|
NM_001289936.2:c.2334G>C
|
NP_001276865.1:p.Thr778=
|
|
NM_001289937.2:c.2379G>C
|
NP_001276866.1:p.Thr793=
|
|
NM_001382782.1:c.2289G>C
|
NP_001369711.1:p.Thr763=
|
|
NM_001382783.1:c.2289G>C
|
NP_001369712.1:p.Thr763=
|
|
NM_001382784.1:c.2496G>C
|
NP_001369713.1:p.Thr832=
|
|
NM_001382785.1:c.2481G>C
|
NP_001369714.1:p.Thr827=
|
|
NM_001382786.1:c.2460G>C
|
NP_001369715.1:p.Thr820=
|
|
NM_001382787.1:c.2454G>C
|
NP_001369716.1:p.Thr818=
|
|
NM_001382788.1:c.2409G>C
|
NP_001369717.1:p.Thr803=
|
|
NM_001382789.1:c.2400G>C
|
NP_001369718.1:p.Thr800=
|
|
NM_001382790.1:c.2376G>C
|
NP_001369719.1:p.Thr792=
|
|
NM_001382791.1:c.2370G>C
|
NP_001369720.1:p.Thr790=
|
|
NM_001382792.1:c.2343G>C
|
NP_001369721.1:p.Thr781=
|
|
NM_001382793.1:c.2337G>C
|
NP_001369722.1:p.Thr779=
|
|
NM_001382794.1:c.2337G>C
|
NP_001369723.1:p.Thr779=
|
|
NM_001382795.1:c.2331G>C
|
NP_001369724.1:p.Thr777=
|
|
NM_001382796.1:c.2379G>C
|
NP_001369725.1:p.Thr793=
|
|
NM_001382797.1:c.2280G>C
|
NP_001369726.1:p.Thr760=
|
|
NM_001382798.1:c.2379G>C
|
NP_001369727.1:p.Thr793=
|
|
NM_001382799.1:c.2199G>C
|
NP_001369728.1:p.Thr733=
|
|
NM_001382800.1:c.2308-252G>C
|
NP_001369729.1:n.2308-252G>C
|
|
NM_001382801.1:c.2331G>C
|
NP_001369730.1:p.Thr777=
|
|
NM_001382802.1:c.2121G>C
|
NP_001369731.1:p.Thr707=
|
|
NM_001382803.1:c.2337G>C
|
NP_001369732.1:p.Thr779=
|
|
NM_001382804.1:c.1551G>C
|
NP_001369733.1:p.Thr517=
|
|
NM_001382805.1:c.2208+1137G>C
|
NP_001369734.1:n.2208+1137G>C
|
|
NM_001382806.1:c.1341G>C
|
NP_001369735.1:p.Thr447=
|
|
NM_004448.4:c.2379G>C
MANE Select
|
NP_004439.2:p.Thr793=
|
|
NR_110535.2:n.2617G>C
|
|
|