ENST00000373275.5:c.565G>T
MANE Select
|
ENSP00000362372.4:p.Asp189Tyr
|
|
ENST00000373275.4:c.565G>T
|
ENSP00000362372.4:p.Asp189Tyr
|
|
ENST00000478415.1:n.777G>T
|
|
|
NM_153252.4:c.565G>T
|
NP_694984.4:p.Asp189Tyr
|
|
XM_005262113.2:c.565G>T
|
XP_005262170.1:p.Asp189Tyr
|
|
XM_011530903.1:c.52G>T
|
XP_011529205.1:p.Asp18Tyr
|
|
XM_011530904.1:c.-772G>T
|
XP_011529206.1:n.-772G>T
|
|
XR_430519.2:n.828G>T
|
|
|
XM_005262113.3:c.565G>T
|
XP_005262170.1:p.Asp189Tyr
|
|
XM_017029384.1:c.-772G>T
|
XP_016884873.1:n.-772G>T
|
|
XM_017029385.2:c.565G>T
|
XP_016884874.1:p.Asp189Tyr
|
|
XR_430519.3:n.830G>T
|
|
|
NM_153252.5:c.565G>T
MANE Select
|
NP_694984.5:p.Asp189Tyr
|
|