ENST00000261208.8:c.844G>T
MANE Select
|
ENSP00000261208.3:p.Asp282Tyr
|
|
ENST00000261208.7:c.844G>T
|
ENSP00000261208.3:p.Asp282Tyr
|
|
ENST00000538703.5:c.844G>T
|
ENSP00000440861.1:p.Asp282Tyr
|
|
ENST00000541929.5:c.220G>T
|
ENSP00000446364.1:p.Asp74Tyr
|
|
ENST00000544080.6:c.*273G>T
|
ENSP00000439385.2:n.*273G>T
|
|
ENST00000546999.5:c.*273G>T
|
ENSP00000447675.1:n.*273G>T
|
|
ENST00000549376.1:n.237G>T
|
|
|
ENST00000551562.1:n.104G>T
|
|
|
ENST00000552509.5:c.808G>T
|
ENSP00000450372.1:p.Asp270Tyr
|
|
NM_001258333.1:c.220G>T
|
NP_001245262.1:p.Asp74Tyr
|
|
NM_001258334.1:c.844G>T
|
NP_001245263.1:p.Asp282Tyr
|
|
NM_002108.3:c.844G>T
|
NP_002099.1:p.Asp282Tyr
|
|
XM_011538249.1:c.4-2164G>T
|
XP_011536551.1:n.4-2164G>T
|
|
XM_011538249.2:c.4-2164G>T
|
XP_011536551.1:n.4-2164G>T
|
|
NM_002108.4:c.844G>T
MANE Select
|
NP_002099.1:p.Asp282Tyr
|
|
NM_001258334.2:c.844G>T
|
NP_001245263.1:p.Asp282Tyr
|
|
NM_001258333.2:c.220G>T
|
NP_001245262.1:p.Asp74Tyr
|
|