ENST00000272602.7:c.560T>C
MANE Select
|
ENSP00000272602.2:p.Ile187Thr
|
|
ENST00000272602.6:c.560T>C
|
ENSP00000272602.2:p.Ile187Thr
|
|
ENST00000393503.2:n.565T>C
|
|
|
ENST00000393504.5:c.560T>C
|
ENSP00000377140.1:p.Ile187Thr
|
|
ENST00000409937.1:c.572T>C
|
ENSP00000386761.1:p.Ile191Thr
|
|
ENST00000436404.6:c.506T>C
|
ENSP00000410070.2:p.Ile169Thr
|
|
NM_001079878.1:c.506T>C
|
NP_001073347.1:p.Ile169Thr
|
|
NM_001298.2:c.560T>C
|
NP_001289.1:p.Ile187Thr
|
|
XM_006712243.2:c.671T>C
|
XP_006712306.1:p.Ile224Thr
|
|
XM_011510554.1:c.725T>C
|
XP_011508856.1:p.Ile242Thr
|
|
XM_011510554.2:c.725T>C
|
XP_011508856.1:p.Ile242Thr
|
|
NM_001079878.2:c.506T>C
|
NP_001073347.1:p.Ile169Thr
|
|
NM_001298.3:c.560T>C
MANE Select
|
NP_001289.1:p.Ile187Thr
|
|