ENST00000684915.1:n.1824A>T
|
|
|
ENST00000688342.1:c.1667A>T
|
ENSP00000508422.1:p.Asp556Val
|
|
ENST00000693213.1:n.945A>T
|
|
|
ENST00000320876.11:c.1667A>T
MANE Select
|
ENSP00000326603.7:p.Asp556Val
|
|
ENST00000320876.10:c.1667A>T
|
ENSP00000326603.6:p.Asp556Val
|
|
ENST00000577300.1:n.18A>T
|
|
|
ENST00000577880.5:c.80A>T
|
ENSP00000463049.1:p.Asp27Val
|
|
NM_015295.2:c.1667A>T
|
NP_056110.2:p.Asp556Val
|
|
XM_011525642.1:c.1667A>T
|
XP_011523944.1:p.Asp556Val
|
|
XM_011525643.1:c.1667A>T
|
XP_011523945.1:p.Asp556Val
|
|
XM_011525644.1:c.1283A>T
|
XP_011523946.1:p.Asp428Val
|
|
XM_011525645.1:c.1103A>T
|
XP_011523947.1:p.Asp368Val
|
|
XM_011525646.1:c.1667A>T
|
XP_011523948.1:p.Asp556Val
|
|
XM_011525647.1:c.1667A>T
|
XP_011523949.1:p.Asp556Val
|
|
XR_430039.1:n.1856A>T
|
|
|
XR_935054.1:n.1856A>T
|
|
|
XR_935055.1:n.1856A>T
|
|
|
XM_011525643.2:c.1667A>T
|
XP_011523945.1:p.Asp556Val
|
|
XM_017025684.1:c.1103A>T
|
XP_016881173.1:p.Asp368Val
|
|
XR_001753172.1:n.1856A>T
|
|
|
XR_001753173.1:n.1856A>T
|
|
|
XR_001753174.1:n.1856A>T
|
|
|
XR_001753175.1:n.1856A>T
|
|
|
XR_001753176.1:n.1856A>T
|
|
|
XR_001753177.1:n.1856A>T
|
|
|
XR_001753178.1:n.1856A>T
|
|
|
XR_001753179.1:n.1856A>T
|
|
|
XR_935055.2:n.1856A>T
|
|
|
NM_015295.3:c.1667A>T
MANE Select
|
NP_056110.2:p.Asp556Val
|
|