|
ENST00000269571.10:c.3254T>G
MANE Select
|
ENSP00000269571.4:p.Val1085Gly
|
|
|
ENST00000269571.9:c.3254T>G
|
ENSP00000269571.4:p.Val1085Gly
|
|
|
ENST00000406381.6:c.3164T>G
|
ENSP00000385185.2:p.Val1055Gly
|
|
|
ENST00000445658.6:c.2426T>G
|
ENSP00000404047.2:p.Val809Gly
|
|
|
ENST00000541774.5:c.3209T>G
|
ENSP00000446466.1:p.Val1070Gly
|
|
|
ENST00000578373.5:c.*3044T>G
|
ENSP00000463427.1:n.*3044T>G
|
|
|
ENST00000584450.5:c.3160-300T>G
|
ENSP00000463714.1:n.3160-300T>G
|
|
|
ENST00000584601.5:c.3164T>G
|
ENSP00000462438.1:p.Val1055Gly
|
|
|
NM_001005862.2:c.3164T>G , LRG_724t1:c.3164T>G
|
NP_001005862.1:p.Val1055Gly
|
|
|
NM_001289936.1:c.3209T>G , LRG_724t4:c.3209T>G
|
NP_001276865.1:p.Val1070Gly
|
|
|
NM_001289937.1:c.3160-300T>G
|
NP_001276866.1:n.3160-300T>G
|
|
|
NM_004448.3:c.3254T>G , LRG_724t2:c.3254T>G
|
NP_004439.2:p.Val1085Gly
|
|
|
NR_110535.1:n.3578T>G
|
|
|
|
XM_024450641.1:c.3392T>G
|
XP_024306409.1:p.Val1131Gly
|
|
|
XM_024450642.1:c.3347T>G
|
XP_024306410.1:p.Val1116Gly
|
|
|
XM_024450643.1:c.3302T>G
|
XP_024306411.1:p.Val1101Gly
|
|
|
NM_001005862.3:c.3164T>G
|
NP_001005862.1:p.Val1055Gly
|
|
|
NM_001289936.2:c.3209T>G
|
NP_001276865.1:p.Val1070Gly
|
|
|
NM_001289937.2:c.3160-300T>G
|
NP_001276866.1:n.3160-300T>G
|
|
|
NM_001382782.1:c.3164T>G
|
NP_001369711.1:p.Val1055Gly
|
|
|
NM_001382783.1:c.3164T>G
|
NP_001369712.1:p.Val1055Gly
|
|
|
NM_001382784.1:c.3371T>G
|
NP_001369713.1:p.Val1124Gly
|
|
|
NM_001382785.1:c.3356T>G
|
NP_001369714.1:p.Val1119Gly
|
|
|
NM_001382786.1:c.3335T>G
|
NP_001369715.1:p.Val1112Gly
|
|
|
NM_001382787.1:c.3329T>G
|
NP_001369716.1:p.Val1110Gly
|
|
|
NM_001382788.1:c.3284T>G
|
NP_001369717.1:p.Val1095Gly
|
|
|
NM_001382789.1:c.3275T>G
|
NP_001369718.1:p.Val1092Gly
|
|
|
NM_001382790.1:c.3251T>G
|
NP_001369719.1:p.Val1084Gly
|
|
|
NM_001382791.1:c.3245T>G
|
NP_001369720.1:p.Val1082Gly
|
|
|
NM_001382792.1:c.3218T>G
|
NP_001369721.1:p.Val1073Gly
|
|
|
NM_001382793.1:c.3212T>G
|
NP_001369722.1:p.Val1071Gly
|
|
|
NM_001382794.1:c.3212T>G
|
NP_001369723.1:p.Val1071Gly
|
|
|
NM_001382795.1:c.3206T>G
|
NP_001369724.1:p.Val1069Gly
|
|
|
NM_001382796.1:c.3167T>G
|
NP_001369725.1:p.Val1056Gly
|
|
|
NM_001382797.1:c.3155T>G
|
NP_001369726.1:p.Val1052Gly
|
|
|
NM_001382798.1:c.3098T>G
|
NP_001369727.1:p.Val1033Gly
|
|
|
NM_001382799.1:c.3074T>G
|
NP_001369728.1:p.Val1025Gly
|
|
|
NM_001382800.1:c.3068T>G
|
NP_001369729.1:p.Val1023Gly
|
|
|
NM_001382801.1:c.3050T>G
|
NP_001369730.1:p.Val1017Gly
|
|
|
NM_001382802.1:c.2996T>G
|
NP_001369731.1:p.Val999Gly
|
|
|
NM_001382803.1:c.3118-300T>G
|
NP_001369732.1:n.3118-300T>G
|
|
|
NM_001382804.1:c.2426T>G
|
NP_001369733.1:p.Val809Gly
|
|
|
NM_001382805.1:c.2303T>G
|
NP_001369734.1:p.Val768Gly
|
|
|
NM_001382806.1:c.2216T>G
|
NP_001369735.1:p.Val739Gly
|
|
|
NM_004448.4:c.3254T>G
MANE Select
|
NP_004439.2:p.Val1085Gly
|
|
|
NR_110535.2:n.3492T>G
|
|
|
