ENST00000302068.9:c.1080T>C
MANE Select
|
ENSP00000306099.4:p.Thr360=
|
|
ENST00000302068.8:c.1080T>C
|
ENSP00000306099.4:p.Thr360=
|
|
ENST00000502545.5:n.939+328T>C
|
|
|
ENST00000509493.1:c.423T>C
|
ENSP00000426757.1:p.Thr141=
|
|
NM_001184741.1:c.903T>C
|
NP_001171670.1:p.Thr301=
|
|
NM_005141.4:c.1080T>C , LRG_558t1:c.1080T>C
|
NP_005132.2:p.Thr360=
|
|
NM_001382759.1:c.948T>C
|
NP_001369688.1:p.Thr316=
|
|
NM_001382760.1:c.1080T>C
|
NP_001369689.1:p.Thr360=
|
|
NM_001382761.1:c.1080T>C
|
NP_001369690.1:p.Thr360=
|
|
NM_001382762.1:c.780T>C
|
NP_001369691.1:p.Thr260=
|
|
NM_001382763.1:c.1071T>C
|
NP_001369692.1:p.Thr357=
|
|
NM_001382764.1:c.1080T>C
|
NP_001369693.1:p.Thr360=
|
|
NM_001382765.1:c.1080T>C
|
NP_001369694.1:p.Thr360=
|
|
NM_005141.5:c.1080T>C
MANE Select
|
NP_005132.2:p.Thr360=
|
|