ENST00000305264.8:c.930G>T
MANE Select
|
ENSP00000302967.3:p.Glu310Asp
|
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ENST00000305264.7:c.930G>T
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ENSP00000302967.3:p.Glu310Asp
|
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ENST00000459727.5:n.233+132G>T
|
|
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ENST00000467533.5:n.599+132G>T
|
|
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ENST00000469207.5:n.9G>T
|
|
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ENST00000469550.6:n.1003G>T
|
|
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ENST00000475549.1:n.261G>T
|
|
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ENST00000486618.1:n.424G>T
|
|
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ENST00000491581.5:n.144G>T
|
|
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ENST00000492407.1:n.767+132G>T
|
|
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NM_003883.3:c.930G>T
|
NP_003874.2:p.Glu310Asp
|
|
XM_011537697.1:c.369G>T
|
XP_011535999.1:p.Glu123Asp
|
|
XR_944336.1:n.1015G>T
|
|
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NM_001355039.1:c.930G>T
|
NP_001341968.1:p.Glu310Asp
|
|
NM_001355040.1:c.471G>T
|
NP_001341969.1:p.Glu157Asp
|
|
NM_001355041.1:c.369G>T
|
NP_001341970.1:p.Glu123Asp
|
|
NR_149164.1:n.996G>T
|
|
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NR_149165.1:n.878G>T
|
|
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NR_149166.1:n.843+132G>T
|
|
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NR_149167.1:n.1011+132G>T
|
|
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NR_149168.1:n.1021G>T
|
|
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NR_149169.1:n.1021G>T
|
|
|
NM_003883.4:c.930G>T
MANE Select
|
NP_003874.2:p.Glu310Asp
|
|
NM_001355039.2:c.930G>T
|
NP_001341968.1:p.Glu310Asp
|
|
NR_149167.2:n.1004+132G>T
|
|
|
NM_001355040.2:c.471G>T
|
NP_001341969.1:p.Glu157Asp
|
|
NM_001355041.2:c.369G>T
|
NP_001341970.1:p.Glu123Asp
|
|
NR_149164.2:n.989G>T
|
|
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NR_149165.2:n.871G>T
|
|
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NR_149166.2:n.836+132G>T
|
|
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NR_149168.2:n.1014G>T
|
|
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NR_149169.2:n.1014G>T
|
|
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