ENST00000320580.9:c.489T>A
MANE Select
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ENSP00000316454.4:p.Ala163=
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|
ENST00000320580.8:c.489T>A
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ENSP00000316454.4:p.Ala163=
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|
ENST00000527224.1:n.613T>A
|
|
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ENST00000527380.1:c.195T>A
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ENSP00000432639.1:p.Ala65=
|
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ENST00000533756.5:c.180T>A
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ENSP00000437150.1:p.Ala60=
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NM_018026.3:c.489T>A
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NP_060496.2:p.Ala163=
|
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XM_011545162.1:c.168T>A
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XP_011543464.1:p.Ala56=
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XM_011545163.1:c.159T>A
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XP_011543465.1:p.Ala53=
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XM_011545164.1:c.150T>A
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XP_011543466.1:p.Ala50=
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XM_011545164.2:c.150T>A
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XP_011543466.1:p.Ala50=
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|
XR_001747924.1:n.700T>A
|
|
|
NM_018026.4:c.489T>A
MANE Select
|
NP_060496.2:p.Ala163=
|
|