ENST00000249806.11:c.608A>T
MANE Select
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ENSP00000249806.5:p.Glu203Val
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ENST00000562767.2:c.84-12066A>T
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ENSP00000456336.1:n.84-12066A>T
|
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ENST00000563917.2:n.450A>T
|
|
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ENST00000565471.6:c.149A>T
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ENSP00000457384.1:p.Glu50Val
|
|
ENST00000635747.1:c.*511A>T
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ENSP00000490627.1:n.*511A>T
|
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ENST00000636212.1:c.*278A>T
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ENSP00000489851.1:n.*278A>T
|
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ENST00000636314.1:c.304A>T
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ENSP00000490295.1:p.Arg102Ter
|
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ENST00000636674.1:n.1710A>T
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|
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ENST00000636964.1:n.2136A>T
|
|
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ENST00000637054.1:c.198+8842A>T
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ENSP00000490807.1:n.198+8842A>T
|
|
ENST00000637329.1:c.577A>T
|
|
|
ENST00000637450.1:c.*262A>T
|
ENSP00000490204.1:n.*262A>T
|
|
ENST00000637494.1:c.320A>T
|
ENSP00000490057.1:p.Glu107Val
|
|
ENST00000637667.1:c.509A>T
|
ENSP00000489843.1:p.Glu170Val
|
|
ENST00000637823.1:c.433A>T
|
|
|
ENST00000637888.1:c.198+8842A>T
|
ENSP00000490546.1:n.198+8842A>T
|
|
ENST00000638076.1:c.*211A>T
|
ENSP00000490373.1:n.*211A>T
|
|
ENST00000638144.1:n.251A>T
|
|
|
ENST00000646164.1:c.38+8842A>T
|
|
|
ENST00000249806.9:c.608A>T
|
ENSP00000249806.5:p.Glu203Val
|
|
ENST00000538696.5:c.704A>T
|
ENSP00000445770.1:p.Glu235Val
|
|
ENST00000562767.1:c.84-12066A>T
|
ENSP00000456336.1:n.84-12066A>T
|
|
ENST00000563917.1:n.508A>T
|
|
|
ENST00000564752.1:c.634A>T
|
ENSP00000457822.1:p.Arg212Ter
|
|
ENST00000565471.5:c.149A>T
|
ENSP00000457384.1:p.Glu50Val
|
|
ENST00000566347.5:c.419A>T
|
ENSP00000457783.1:p.Glu140Val
|
|
ENST00000567060.5:c.*6A>T
|
ENSP00000454818.1:n.*6A>T
|
|
NM_017882.2:c.608A>T
|
NP_060352.1:p.Glu203Val
|
|
XR_931861.1:n.830A>T
|
|
|
NM_017882.3:c.608A>T
MANE Select
|
NP_060352.1:p.Glu203Val
|
|