ENST00000322213.9:c.3255T>C
MANE Select
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ENSP00000323421.3:p.Tyr1085=
|
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ENST00000674590.1:c.2487T>C
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ENSP00000502626.1:p.Tyr829=
|
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ENST00000675504.1:c.3189T>C
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ENSP00000502524.1:p.Tyr1063=
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ENST00000322213.8:c.3255T>C
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ENSP00000323421.3:p.Tyr1085=
|
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ENST00000375340.10:c.3189T>C
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ENSP00000364489.7:p.Tyr1063=
|
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ENST00000469129.1:n.111T>C
|
|
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ENST00000470241.2:c.545T>C
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|
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NM_001281463.1:c.3189T>C , LRG_773t1:c.3189T>C
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NP_001268392.1:p.Tyr1063=
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NM_006306.3:c.3255T>C , LRG_773t2:c.3255T>C
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NP_006297.2:p.Tyr1085=
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NM_006306.4:c.3255T>C
MANE Select
|
NP_006297.2:p.Tyr1085=
|
|