ENST00000301244.12:c.303C>G
MANE Select
|
ENSP00000301244.5:p.Thr101=
|
|
ENST00000301244.11:c.303C>G
|
ENSP00000301244.5:p.Thr101=
|
|
ENST00000454580.7:c.132C>G
|
ENSP00000389788.2:p.Thr44=
|
|
ENST00000587090.5:c.153C>G
|
ENSP00000466407.1:p.Thr51=
|
|
ENST00000587516.5:c.278-1237C>G
|
ENSP00000465721.1:n.278-1237C>G
|
|
ENST00000590210.1:n.500C>G
|
|
|
ENST00000590510.5:c.153C>G
|
ENSP00000465301.1:p.Thr51=
|
|
ENST00000592007.1:c.153C>G
|
ENSP00000465561.1:p.Thr51=
|
|
NM_001166103.1:c.132C>G
|
NP_001159575.1:p.Thr44=
|
|
NM_021102.3:c.303C>G
|
NP_066925.1:p.Thr101=
|
|
NM_021102.4:c.303C>G
MANE Select
|
NP_066925.1:p.Thr101=
|
|
NM_001166103.2:c.132C>G
|
NP_001159575.1:p.Thr44=
|
|