ENST00000682114.1:c.246T>A
|
ENSP00000507245.1:p.Ala82=
|
|
ENST00000682478.1:n.222T>A
|
|
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ENST00000683576.1:n.222T>A
|
|
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ENST00000683627.1:c.246T>A
|
ENSP00000507533.1:p.Ala82=
|
|
ENST00000684082.1:c.246T>A
|
ENSP00000508266.1:p.Ala82=
|
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ENST00000684633.1:n.218T>A
|
|
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ENST00000684678.1:c.242T>A
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ENSP00000507059.1:n.242T>A
|
|
ENST00000369842.9:c.246T>A
MANE Select
|
ENSP00000358857.4:p.Ala82=
|
|
ENST00000369835.3:c.141T>A
|
ENSP00000358850.3:p.Ala47=
|
|
ENST00000369842.8:c.246T>A
|
ENSP00000358857.4:p.Ala82=
|
|
ENST00000428228.5:c.*151T>A
|
ENSP00000401081.1:n.*151T>A
|
|
ENST00000468294.5:n.206T>A
|
|
|
ENST00000485261.1:n.222T>A
|
|
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ENST00000486738.5:n.390T>A
|
|
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ENST00000492448.1:n.229T>A
|
|
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ENST00000494443.5:n.303T>A
|
|
|
NM_000117.2:c.246T>A , LRG_745t1:c.246T>A
|
NP_000108.1:p.Ala82=
|
|
XM_024452349.1:c.38T>A
|
XP_024308117.1:p.Leu13His
|
|
NM_000117.3:c.246T>A
MANE Select
|
NP_000108.1:p.Ala82=
|
|