ENST00000642496.1:c.3955A>T
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ENST00000644397.2:c.5096A>T
MANE Select
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ENSP00000495195.1:p.Glu1699Val
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ENST00000373965.6:c.4907A>T
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ENSP00000363076.3:p.Glu1636Val
|
|
ENST00000414778.5:c.4904A>T
|
ENSP00000410304.2:p.Glu1635Val
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ENST00000495484.5:c.1124A>T
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ENSP00000480780.1:p.Glu375Val
|
|
ENST00000614895.4:c.4919A>T
|
ENSP00000478512.1:p.Glu1640Val
|
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ENST00000616114.4:c.4901A>T
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ENSP00000483745.1:p.Glu1634Val
|
|
ENST00000618301.4:c.1256A>T
|
ENSP00000482780.1:p.Glu419Val
|
|
ENST00000621708.4:c.4922A>T
|
ENSP00000484454.1:p.Glu1641Val
|
|
NM_001142771.1:c.4922A>T
|
NP_001136243.1:p.Glu1641Val
|
|
NM_001142772.1:c.4907A>T
|
NP_001136244.1:p.Glu1636Val
|
|
NM_001354420.1:c.4901A>T
|
NP_001341349.1:p.Glu1634Val
|
|
NM_001354429.1:c.5030A>T
|
NP_001341358.1:p.Glu1677Val
|
|
XR_001747192.2:n.11388A>T
|
|
|
XR_001747193.2:n.11379A>T
|
|
|
NM_001142771.2:c.4922A>T
|
NP_001136243.1:p.Glu1641Val
|
|
NM_001142772.2:c.4907A>T
|
NP_001136244.1:p.Glu1636Val
|
|
NM_001354420.2:c.4901A>T
|
NP_001341349.1:p.Glu1634Val
|
|
NM_001354429.2:c.5030A>T
|
NP_001341358.1:p.Glu1677Val
|
|
NM_001384140.1:c.5096A>T
MANE Select
|
NP_001371069.1:p.Glu1699Val
|
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