|
NM_006206.6:c.2524G>T
MANE Select
|
NP_006197.1:p.Asp842Tyr
|
|
ENST00000257290.10:c.2524G>T
MANE Select
|
ENSP00000257290.5:p.Asp842Tyr
|
|
NM_001347828.1:c.2599G>T
|
NP_001334757.1:p.Asp867Tyr
|
|
NM_001347828.2:c.2599G>T
|
NP_001334757.1:p.Asp867Tyr
|
|
NM_001347829.1:c.2524G>T
|
NP_001334758.1:p.Asp842Tyr
|
|
NM_001347829.2:c.2524G>T
|
NP_001334758.1:p.Asp842Tyr
|
|
NM_001347830.1:c.2563G>T
|
NP_001334759.1:p.Asp855Tyr
|
|
NM_001347830.2:c.2563G>T
|
NP_001334759.1:p.Asp855Tyr
|
|
NM_006206.4:c.2524G>T , LRG_309t1:c.2524G>T
|
NP_006197.1:p.Asp842Tyr
|
|
NM_006206.5:c.2524G>T
|
NP_006197.1:p.Asp842Tyr
|
|
ENST00000257290.9:c.2524G>T
|
ENSP00000257290.5:p.Asp842Tyr
|
|
ENST00000507166.5:c.1804G>T
|
ENSP00000423325.1:p.Asp602Tyr
|
|
XM_005265743.1:c.2524G>T
|
XP_005265800.1:p.Asp842Tyr
|
|
XM_006714039.2:c.2599G>T
|
XP_006714102.1:p.Asp867Tyr
|
|
XM_011534385.1:c.2524G>T
|
XP_011532687.1:p.Asp842Tyr
|
|
XM_011534386.1:c.2524G>T
|
XP_011532688.1:p.Asp842Tyr
|
