ENST00000642496.1:c.3953G>T
|
|
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ENST00000644397.2:c.5094G>T
MANE Select
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ENSP00000495195.1:p.Gln1698His
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ENST00000373965.6:c.4905G>T
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ENSP00000363076.3:p.Gln1635His
|
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ENST00000414778.5:c.4902G>T
|
ENSP00000410304.2:p.Gln1634His
|
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ENST00000495484.5:c.1122G>T
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ENSP00000480780.1:p.Gln374His
|
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ENST00000614895.4:c.4917G>T
|
ENSP00000478512.1:p.Gln1639His
|
|
ENST00000616114.4:c.4899G>T
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ENSP00000483745.1:p.Gln1633His
|
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ENST00000618301.4:c.1254G>T
|
ENSP00000482780.1:p.Gln418His
|
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ENST00000621708.4:c.4920G>T
|
ENSP00000484454.1:p.Gln1640His
|
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NM_001142771.1:c.4920G>T
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NP_001136243.1:p.Gln1640His
|
|
NM_001142772.1:c.4905G>T
|
NP_001136244.1:p.Gln1635His
|
|
NM_001354420.1:c.4899G>T
|
NP_001341349.1:p.Gln1633His
|
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NM_001354429.1:c.5028G>T
|
NP_001341358.1:p.Gln1676His
|
|
XR_001747192.2:n.11386G>T
|
|
|
XR_001747193.2:n.11377G>T
|
|
|
NM_001142771.2:c.4920G>T
|
NP_001136243.1:p.Gln1640His
|
|
NM_001142772.2:c.4905G>T
|
NP_001136244.1:p.Gln1635His
|
|
NM_001354420.2:c.4899G>T
|
NP_001341349.1:p.Gln1633His
|
|
NM_001354429.2:c.5028G>T
|
NP_001341358.1:p.Gln1676His
|
|
NM_001384140.1:c.5094G>T
MANE Select
|
NP_001371069.1:p.Gln1698His
|
|