|
ENST00000269571.10:c.3371C>G
MANE Select
|
ENSP00000269571.4:p.Thr1124Ser
|
|
|
ENST00000269571.9:c.3371C>G
|
ENSP00000269571.4:p.Thr1124Ser
|
|
|
ENST00000406381.6:c.3281C>G
|
ENSP00000385185.2:p.Thr1094Ser
|
|
|
ENST00000445658.6:c.2543C>G
|
ENSP00000404047.2:p.Thr848Ser
|
|
|
ENST00000541774.5:c.3326C>G
|
ENSP00000446466.1:p.Thr1109Ser
|
|
|
ENST00000578373.5:c.*3161C>G
|
ENSP00000463427.1:n.*3161C>G
|
|
|
ENST00000584450.5:c.3160-183C>G
|
ENSP00000463714.1:n.3160-183C>G
|
|
|
ENST00000584601.5:c.3281C>G
|
ENSP00000462438.1:p.Thr1094Ser
|
|
|
NM_001005862.2:c.3281C>G , LRG_724t1:c.3281C>G
|
NP_001005862.1:p.Thr1094Ser
|
|
|
NM_001289936.1:c.3326C>G , LRG_724t4:c.3326C>G
|
NP_001276865.1:p.Thr1109Ser
|
|
|
NM_001289937.1:c.3160-183C>G
|
NP_001276866.1:n.3160-183C>G
|
|
|
NM_004448.3:c.3371C>G , LRG_724t2:c.3371C>G
|
NP_004439.2:p.Thr1124Ser
|
|
|
NR_110535.1:n.3695C>G
|
|
|
|
XM_024450641.1:c.3509C>G
|
XP_024306409.1:p.Thr1170Ser
|
|
|
XM_024450642.1:c.3464C>G
|
XP_024306410.1:p.Thr1155Ser
|
|
|
XM_024450643.1:c.3419C>G
|
XP_024306411.1:p.Thr1140Ser
|
|
|
NM_001005862.3:c.3281C>G
|
NP_001005862.1:p.Thr1094Ser
|
|
|
NM_001289936.2:c.3326C>G
|
NP_001276865.1:p.Thr1109Ser
|
|
|
NM_001289937.2:c.3160-183C>G
|
NP_001276866.1:n.3160-183C>G
|
|
|
NM_001382782.1:c.3281C>G
|
NP_001369711.1:p.Thr1094Ser
|
|
|
NM_001382783.1:c.3281C>G
|
NP_001369712.1:p.Thr1094Ser
|
|
|
NM_001382784.1:c.3488C>G
|
NP_001369713.1:p.Thr1163Ser
|
|
|
NM_001382785.1:c.3473C>G
|
NP_001369714.1:p.Thr1158Ser
|
|
|
NM_001382786.1:c.3452C>G
|
NP_001369715.1:p.Thr1151Ser
|
|
|
NM_001382787.1:c.3446C>G
|
NP_001369716.1:p.Thr1149Ser
|
|
|
NM_001382788.1:c.3401C>G
|
NP_001369717.1:p.Thr1134Ser
|
|
|
NM_001382789.1:c.3392C>G
|
NP_001369718.1:p.Thr1131Ser
|
|
|
NM_001382790.1:c.3368C>G
|
NP_001369719.1:p.Thr1123Ser
|
|
|
NM_001382791.1:c.3362C>G
|
NP_001369720.1:p.Thr1121Ser
|
|
|
NM_001382792.1:c.3335C>G
|
NP_001369721.1:p.Thr1112Ser
|
|
|
NM_001382793.1:c.3329C>G
|
NP_001369722.1:p.Thr1110Ser
|
|
|
NM_001382794.1:c.3329C>G
|
NP_001369723.1:p.Thr1110Ser
|
|
|
NM_001382795.1:c.3323C>G
|
NP_001369724.1:p.Thr1108Ser
|
|
|
NM_001382796.1:c.3284C>G
|
NP_001369725.1:p.Thr1095Ser
|
|
|
NM_001382797.1:c.3272C>G
|
NP_001369726.1:p.Thr1091Ser
|
|
|
NM_001382798.1:c.3215C>G
|
NP_001369727.1:p.Thr1072Ser
|
|
|
NM_001382799.1:c.3191C>G
|
NP_001369728.1:p.Thr1064Ser
|
|
|
NM_001382800.1:c.3185C>G
|
NP_001369729.1:p.Thr1062Ser
|
|
|
NM_001382801.1:c.3167C>G
|
NP_001369730.1:p.Thr1056Ser
|
|
|
NM_001382802.1:c.3113C>G
|
NP_001369731.1:p.Thr1038Ser
|
|
|
NM_001382803.1:c.3118-183C>G
|
NP_001369732.1:n.3118-183C>G
|
|
|
NM_001382804.1:c.2543C>G
|
NP_001369733.1:p.Thr848Ser
|
|
|
NM_001382805.1:c.2420C>G
|
NP_001369734.1:p.Thr807Ser
|
|
|
NM_001382806.1:c.2333C>G
|
NP_001369735.1:p.Thr778Ser
|
|
|
NM_004448.4:c.3371C>G
MANE Select
|
NP_004439.2:p.Thr1124Ser
|
|
|
NR_110535.2:n.3609C>G
|
|
|
