ENST00000355832.10:c.1802G>T
MANE Select
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ENSP00000348089.5:p.Gly601Val
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ENST00000681632.1:n.1880G>T
|
|
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ENST00000681659.1:c.1643G>T
|
ENSP00000505631.1:p.Gly548Val
|
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ENST00000355832.9:c.1802G>T
|
ENSP00000348089.5:p.Gly601Val
|
|
ENST00000475116.1:n.275+7402G>T
|
|
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ENST00000623073.3:c.203G>T
|
ENSP00000485650.1:p.Gly68Val
|
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ENST00000623115.3:c.-70+7402G>T
|
ENSP00000485321.1:n.-70+7402G>T
|
|
ENST00000623318.1:c.203G>T
|
ENSP00000485423.1:p.Gly68Val
|
|
NM_000124.3:c.1802G>T
|
NP_000115.1:p.Gly601Val
|
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NM_001346440.1:c.1802G>T
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NP_001333369.1:p.Gly601Val
|
|
NM_000124.4:c.1802G>T
MANE Select
|
NP_000115.1:p.Gly601Val
|
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NM_001346440.2:c.1802G>T
|
NP_001333369.1:p.Gly601Val
|
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