|
ENST00000269571.10:c.2363T>G
MANE Select
|
ENSP00000269571.4:p.Ile788Ser
|
|
|
ENST00000269571.9:c.2363T>G
|
ENSP00000269571.4:p.Ile788Ser
|
|
|
ENST00000406381.6:c.2273T>G
|
ENSP00000385185.2:p.Ile758Ser
|
|
|
ENST00000445658.6:c.1535T>G
|
ENSP00000404047.2:p.Ile512Ser
|
|
|
ENST00000541774.5:c.2318T>G
|
ENSP00000446466.1:p.Ile773Ser
|
|
|
ENST00000578373.5:c.*2153T>G
|
ENSP00000463427.1:n.*2153T>G
|
|
|
ENST00000580074.1:c.469T>G
|
|
|
|
ENST00000583038.5:n.3497T>G
|
|
|
|
ENST00000584450.5:c.2363T>G
|
ENSP00000463714.1:p.Ile788Ser
|
|
|
ENST00000584601.5:c.2273T>G
|
ENSP00000462438.1:p.Ile758Ser
|
|
|
NM_001005862.2:c.2273T>G , LRG_724t1:c.2273T>G
|
NP_001005862.1:p.Ile758Ser
|
|
|
NM_001289936.1:c.2318T>G , LRG_724t4:c.2318T>G
|
NP_001276865.1:p.Ile773Ser
|
|
|
NM_001289937.1:c.2363T>G
|
NP_001276866.1:p.Ile788Ser
|
|
|
NM_004448.3:c.2363T>G , LRG_724t2:c.2363T>G
|
NP_004439.2:p.Ile788Ser
|
|
|
NR_110535.1:n.2687T>G
|
|
|
|
XM_024450641.1:c.2501T>G
|
XP_024306409.1:p.Ile834Ser
|
|
|
XM_024450642.1:c.2456T>G
|
XP_024306410.1:p.Ile819Ser
|
|
|
XM_024450643.1:c.2411T>G
|
XP_024306411.1:p.Ile804Ser
|
|
|
NM_001005862.3:c.2273T>G
|
NP_001005862.1:p.Ile758Ser
|
|
|
NM_001289936.2:c.2318T>G
|
NP_001276865.1:p.Ile773Ser
|
|
|
NM_001289937.2:c.2363T>G
|
NP_001276866.1:p.Ile788Ser
|
|
|
NM_001382782.1:c.2273T>G
|
NP_001369711.1:p.Ile758Ser
|
|
|
NM_001382783.1:c.2273T>G
|
NP_001369712.1:p.Ile758Ser
|
|
|
NM_001382784.1:c.2480T>G
|
NP_001369713.1:p.Ile827Ser
|
|
|
NM_001382785.1:c.2465T>G
|
NP_001369714.1:p.Ile822Ser
|
|
|
NM_001382786.1:c.2444T>G
|
NP_001369715.1:p.Ile815Ser
|
|
|
NM_001382787.1:c.2438T>G
|
NP_001369716.1:p.Ile813Ser
|
|
|
NM_001382788.1:c.2393T>G
|
NP_001369717.1:p.Ile798Ser
|
|
|
NM_001382789.1:c.2384T>G
|
NP_001369718.1:p.Ile795Ser
|
|
|
NM_001382790.1:c.2360T>G
|
NP_001369719.1:p.Ile787Ser
|
|
|
NM_001382791.1:c.2354T>G
|
NP_001369720.1:p.Ile785Ser
|
|
|
NM_001382792.1:c.2327T>G
|
NP_001369721.1:p.Ile776Ser
|
|
|
NM_001382793.1:c.2321T>G
|
NP_001369722.1:p.Ile774Ser
|
|
|
NM_001382794.1:c.2321T>G
|
NP_001369723.1:p.Ile774Ser
|
|
|
NM_001382795.1:c.2315T>G
|
NP_001369724.1:p.Ile772Ser
|
|
|
NM_001382796.1:c.2363T>G
|
NP_001369725.1:p.Ile788Ser
|
|
|
NM_001382797.1:c.2264T>G
|
NP_001369726.1:p.Ile755Ser
|
|
|
NM_001382798.1:c.2363T>G
|
NP_001369727.1:p.Ile788Ser
|
|
|
NM_001382799.1:c.2183T>G
|
NP_001369728.1:p.Ile728Ser
|
|
|
NM_001382800.1:c.2308-268T>G
|
NP_001369729.1:n.2308-268T>G
|
|
|
NM_001382801.1:c.2315T>G
|
NP_001369730.1:p.Ile772Ser
|
|
|
NM_001382802.1:c.2105T>G
|
NP_001369731.1:p.Ile702Ser
|
|
|
NM_001382803.1:c.2321T>G
|
NP_001369732.1:p.Ile774Ser
|
|
|
NM_001382804.1:c.1535T>G
|
NP_001369733.1:p.Ile512Ser
|
|
|
NM_001382805.1:c.2208+1121T>G
|
NP_001369734.1:n.2208+1121T>G
|
|
|
NM_001382806.1:c.1325T>G
|
NP_001369735.1:p.Ile442Ser
|
|
|
NM_004448.4:c.2363T>G
MANE Select
|
NP_004439.2:p.Ile788Ser
|
|
|
NR_110535.2:n.2601T>G
|
|
|
