ENST00000403733.8:c.3253G>T
MANE Select
|
ENSP00000384222.3:p.Asp1085Tyr
|
|
ENST00000403733.7:c.3253G>T
|
ENSP00000384222.3:p.Asp1085Tyr
|
|
ENST00000427431.5:c.*2645G>T
|
ENSP00000393342.1:n.*2645G>T
|
|
ENST00000438543.5:c.*1049G>T
|
ENSP00000413521.1:n.*1049G>T
|
|
ENST00000448232.6:c.3325G>T
|
ENSP00000398577.2:p.Asp1109Tyr
|
|
ENST00000504005.5:c.2299G>T
|
ENSP00000427569.1:p.Asp767Tyr
|
|
ENST00000508747.1:c.637G>T
|
ENSP00000420835.1:p.Asp213Tyr
|
|
ENST00000513834.5:c.3106G>T
|
ENSP00000425054.1:p.Asp1036Tyr
|
|
NM_024949.5:c.3253G>T
|
NP_079225.5:p.Asp1085Tyr
|
|
XM_011532269.1:c.3325G>T
|
XP_011530571.1:p.Asp1109Tyr
|
|
XM_011532269.3:c.3325G>T
|
XP_011530571.1:p.Asp1109Tyr
|
|
XM_024454225.1:c.3031G>T
|
XP_024309993.1:p.Asp1011Tyr
|
|
NM_024949.6:c.3253G>T
MANE Select
|
NP_079225.5:p.Asp1085Tyr
|
|