ENST00000269571.10:c.3498T>C
MANE Select
|
ENSP00000269571.4:p.Thr1166=
|
|
ENST00000269571.9:c.3498T>C
|
ENSP00000269571.4:p.Thr1166=
|
|
ENST00000406381.6:c.3408T>C
|
ENSP00000385185.2:p.Thr1136=
|
|
ENST00000445658.6:c.2670T>C
|
ENSP00000404047.2:p.Thr890=
|
|
ENST00000541774.5:c.3453T>C
|
ENSP00000446466.1:p.Thr1151=
|
|
ENST00000578373.5:c.*3288T>C
|
ENSP00000463427.1:n.*3288T>C
|
|
ENST00000584450.5:c.*77T>C
|
ENSP00000463714.1:n.*77T>C
|
|
ENST00000584601.5:c.3408T>C
|
ENSP00000462438.1:p.Thr1136=
|
|
NM_001005862.2:c.3408T>C , LRG_724t1:c.3408T>C
|
NP_001005862.1:p.Thr1136=
|
|
NM_001289936.1:c.3453T>C , LRG_724t4:c.3453T>C
|
NP_001276865.1:p.Thr1151=
|
|
NM_001289937.1:c.*77T>C
|
NP_001276866.1:n.*77T>C
|
|
NM_004448.3:c.3498T>C , LRG_724t2:c.3498T>C
|
NP_004439.2:p.Thr1166=
|
|
NR_110535.1:n.3822T>C
|
|
|
XM_024450641.1:c.3636T>C
|
XP_024306409.1:p.Thr1212=
|
|
XM_024450642.1:c.3591T>C
|
XP_024306410.1:p.Thr1197=
|
|
XM_024450643.1:c.3546T>C
|
XP_024306411.1:p.Thr1182=
|
|
NM_001005862.3:c.3408T>C
|
NP_001005862.1:p.Thr1136=
|
|
NM_001289936.2:c.3453T>C
|
NP_001276865.1:p.Thr1151=
|
|
NM_001289937.2:c.*77T>C
|
NP_001276866.1:n.*77T>C
|
|
NM_001382782.1:c.3408T>C
|
NP_001369711.1:p.Thr1136=
|
|
NM_001382783.1:c.3408T>C
|
NP_001369712.1:p.Thr1136=
|
|
NM_001382784.1:c.3615T>C
|
NP_001369713.1:p.Thr1205=
|
|
NM_001382785.1:c.3600T>C
|
NP_001369714.1:p.Thr1200=
|
|
NM_001382786.1:c.3579T>C
|
NP_001369715.1:p.Thr1193=
|
|
NM_001382787.1:c.3573T>C
|
NP_001369716.1:p.Thr1191=
|
|
NM_001382788.1:c.3528T>C
|
NP_001369717.1:p.Thr1176=
|
|
NM_001382789.1:c.3519T>C
|
NP_001369718.1:p.Thr1173=
|
|
NM_001382790.1:c.3495T>C
|
NP_001369719.1:p.Thr1165=
|
|
NM_001382791.1:c.3489T>C
|
NP_001369720.1:p.Thr1163=
|
|
NM_001382792.1:c.3462T>C
|
NP_001369721.1:p.Thr1154=
|
|
NM_001382793.1:c.3456T>C
|
NP_001369722.1:p.Thr1152=
|
|
NM_001382794.1:c.3456T>C
|
NP_001369723.1:p.Thr1152=
|
|
NM_001382795.1:c.3450T>C
|
NP_001369724.1:p.Thr1150=
|
|
NM_001382796.1:c.3411T>C
|
NP_001369725.1:p.Thr1137=
|
|
NM_001382797.1:c.3399T>C
|
NP_001369726.1:p.Thr1133=
|
|
NM_001382798.1:c.3342T>C
|
NP_001369727.1:p.Thr1114=
|
|
NM_001382799.1:c.3318T>C
|
NP_001369728.1:p.Thr1106=
|
|
NM_001382800.1:c.3312T>C
|
NP_001369729.1:p.Thr1104=
|
|
NM_001382801.1:c.3294T>C
|
NP_001369730.1:p.Thr1098=
|
|
NM_001382802.1:c.3240T>C
|
NP_001369731.1:p.Thr1080=
|
|
NM_001382803.1:c.*77T>C
|
NP_001369732.1:n.*77T>C
|
|
NM_001382804.1:c.2670T>C
|
NP_001369733.1:p.Thr890=
|
|
NM_001382805.1:c.2547T>C
|
NP_001369734.1:p.Thr849=
|
|
NM_001382806.1:c.2460T>C
|
NP_001369735.1:p.Thr820=
|
|
NM_004448.4:c.3498T>C
MANE Select
|
NP_004439.2:p.Thr1166=
|
|
NR_110535.2:n.3736T>C
|
|
|