ENST00000262629.9:c.183G>A
MANE Select
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ENSP00000262629.3:p.Val61=
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ENST00000262629.8:c.183G>A
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ENSP00000262629.3:p.Val61=
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ENST00000424586.7:c.150G>A
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ENSP00000402371.3:p.Val50=
|
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ENST00000544690.6:c.150G>A
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ENSP00000445332.1:p.Val50=
|
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ENST00000585626.1:n.250G>A
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|
|
ENST00000585901.6:c.183G>A
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ENSP00000468608.1:p.Val61=
|
|
ENST00000586946.1:c.*68G>A
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ENSP00000465656.1:n.*68G>A
|
|
ENST00000587837.5:c.*68G>A
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ENSP00000465081.1:n.*68G>A
|
|
ENST00000588439.1:n.327G>A
|
|
|
ENST00000589517.1:c.183G>A
|
ENSP00000468447.1:p.Val61=
|
|
NM_001173514.1:c.150G>A
|
NP_001166985.1:p.Val50=
|
|
NM_001173515.1:c.150G>A
|
NP_001166986.1:p.Val50=
|
|
NM_003332.3:c.183G>A , LRG_607t1:c.183G>A
|
NP_003323.1:p.Val61=
|
|
NM_198125.2:c.183G>A
|
NP_937758.1:p.Val61=
|
|
NR_033390.1:n.224G>A
|
|
|
NM_001173514.2:c.150G>A
|
NP_001166985.1:p.Val50=
|
|
NM_001173515.2:c.150G>A
|
NP_001166986.1:p.Val50=
|
|
NM_003332.4:c.183G>A
MANE Select
|
NP_003323.1:p.Val61=
|
|
NM_198125.3:c.183G>A
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NP_937758.1:p.Val61=
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|
NR_033390.2:n.210G>A
|
|
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