ENST00000261208.8:c.853T=
MANE Select
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ENSP00000261208.3:p.Tyr285=
|
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ENST00000261208.7:c.853T=
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ENSP00000261208.3:p.Tyr285=
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|
ENST00000538703.5:c.853T=
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ENSP00000440861.1:p.Tyr285=
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ENST00000541929.5:c.229T=
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ENSP00000446364.1:p.Tyr77=
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ENST00000544080.6:c.*282T=
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ENSP00000439385.2:n.*282T=
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ENST00000546999.5:c.*282T=
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ENSP00000447675.1:n.*282T=
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ENST00000549376.1:n.246T=
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|
|
ENST00000551562.1:n.113T=
|
|
|
ENST00000552509.5:c.817T=
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ENSP00000450372.1:p.Tyr273=
|
|
NM_001258333.1:c.229T=
|
NP_001245262.1:p.Tyr77=
|
|
NM_001258334.1:c.853T=
|
NP_001245263.1:p.Tyr285=
|
|
NM_002108.3:c.853T=
|
NP_002099.1:p.Tyr285=
|
|
XM_011538249.1:c.4-2155T=
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XP_011536551.1:n.4-2155T=
|
|
XM_011538249.2:c.4-2155T=
|
XP_011536551.1:n.4-2155T=
|
|
NM_002108.4:c.853T=
MANE Select
|
NP_002099.1:p.Tyr285=
|
|
NM_001258334.2:c.853T=
|
NP_001245263.1:p.Tyr285=
|
|
NM_001258333.2:c.229T=
|
NP_001245262.1:p.Tyr77=
|
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