ENST00000336079.8:c.593A>C
MANE Select
|
ENSP00000336725.3:p.Tyr198Ser
|
|
ENST00000336079.7:c.593A>C
|
ENSP00000336725.3:p.Tyr198Ser
|
|
ENST00000360160.8:c.593A>C
|
ENSP00000353284.4:p.Tyr198Ser
|
|
ENST00000440554.1:c.584A>C
|
ENSP00000400377.1:p.Tyr195Ser
|
|
ENST00000454054.5:c.593A>C
|
ENSP00000398953.1:p.Tyr198Ser
|
|
ENST00000463199.1:n.111A>C
|
|
|
ENST00000469101.1:n.479A>C
|
|
|
ENST00000472510.5:n.156A>C
|
|
|
NM_001122665.2:c.593A>C
|
NP_001116137.1:p.Tyr198Ser
|
|
NM_001302552.1:c.584A>C
|
NP_001289481.1:p.Tyr195Ser
|
|
NM_004660.4:c.593A>C
|
NP_004651.2:p.Tyr198Ser
|
|
XM_006724878.1:c.593A>C
|
XP_006724941.1:p.Tyr198Ser
|
|
XM_011531471.1:c.593A>C
|
XP_011529773.1:p.Tyr198Ser
|
|
NM_001122665.3:c.593A>C
|
NP_001116137.1:p.Tyr198Ser
|
|
NM_001302552.2:c.584A>C
|
NP_001289481.1:p.Tyr195Ser
|
|
NM_001324195.1:c.593A>C
|
NP_001311124.1:p.Tyr198Ser
|
|
NR_136716.1:n.744A>C
|
|
|
NR_136717.1:n.824A>C
|
|
|
NR_136718.1:n.824A>C
|
|
|
NR_136719.1:n.614A>C
|
|
|
NR_136720.1:n.744A>C
|
|
|
NR_136721.1:n.672A>C
|
|
|
NR_136722.1:n.739A>C
|
|
|
NR_136723.1:n.739A>C
|
|
|
NR_136724.1:n.659A>C
|
|
|
XR_001756014.2:n.697A>C
|
|
|
NM_004660.5:c.593A>C
MANE Select
|
NP_004651.2:p.Tyr198Ser
|
|
NM_001302552.3:c.584A>C
|
NP_001289481.1:p.Tyr195Ser
|
|
NM_001324195.2:c.593A>C
|
NP_001311124.1:p.Tyr198Ser
|
|
NR_136716.2:n.662A>C
|
|
|
NR_136717.2:n.742A>C
|
|
|
NR_136718.2:n.742A>C
|
|
|
NR_136719.2:n.532A>C
|
|
|
NR_136720.2:n.662A>C
|
|
|
NR_136721.2:n.662A>C
|
|
|