ENST00000642496.1:c.3949A>T
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ENST00000644397.2:c.5090A>T
MANE Select
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ENSP00000495195.1:p.Glu1697Val
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ENST00000373965.6:c.4901A>T
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ENSP00000363076.3:p.Glu1634Val
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ENST00000414778.5:c.4898A>T
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ENSP00000410304.2:p.Glu1633Val
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ENST00000495484.5:c.1118A>T
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ENSP00000480780.1:p.Glu373Val
|
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ENST00000614895.4:c.4913A>T
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ENSP00000478512.1:p.Glu1638Val
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ENST00000616114.4:c.4895A>T
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ENSP00000483745.1:p.Glu1632Val
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ENST00000618301.4:c.1250A>T
|
ENSP00000482780.1:p.Glu417Val
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ENST00000621708.4:c.4916A>T
|
ENSP00000484454.1:p.Glu1639Val
|
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NM_001142771.1:c.4916A>T
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NP_001136243.1:p.Glu1639Val
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NM_001142772.1:c.4901A>T
|
NP_001136244.1:p.Glu1634Val
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NM_001354420.1:c.4895A>T
|
NP_001341349.1:p.Glu1632Val
|
|
NM_001354429.1:c.5024A>T
|
NP_001341358.1:p.Glu1675Val
|
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XR_001747192.2:n.11382A>T
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|
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XR_001747193.2:n.11373A>T
|
|
|
NM_001142771.2:c.4916A>T
|
NP_001136243.1:p.Glu1639Val
|
|
NM_001142772.2:c.4901A>T
|
NP_001136244.1:p.Glu1634Val
|
|
NM_001354420.2:c.4895A>T
|
NP_001341349.1:p.Glu1632Val
|
|
NM_001354429.2:c.5024A>T
|
NP_001341358.1:p.Glu1675Val
|
|
NM_001384140.1:c.5090A>T
MANE Select
|
NP_001371069.1:p.Glu1697Val
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