ENST00000313601.11:c.482A>T
MANE Select
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ENSP00000312999.6:p.Glu161Val
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ENST00000266027.9:c.326A>T
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ENSP00000266027.6:p.Glu109Val
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ENST00000313601.10:c.482A>T
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ENSP00000312999.6:p.Glu161Val
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ENST00000422163.5:c.434A>T
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ENSP00000406871.1:p.Glu145Val
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ENST00000440628.5:c.326A>T
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ENSP00000395736.1:p.Glu109Val
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ENST00000441156.5:c.*10A>T
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ENSP00000394321.1:n.*10A>T
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ENST00000446079.5:c.*117A>T
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ENSP00000406065.1:n.*117A>T
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ENST00000451956.1:c.371A>T
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ENSP00000406369.1:p.Glu124Val
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ENST00000468422.1:n.49A>T
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ENST00000490122.5:n.1309A>T
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ENST00000491100.5:n.2298A>T
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NM_001166425.1:c.371A>T
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NP_001159897.1:p.Glu124Val
|
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NM_001282617.1:c.326A>T
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NP_001269546.1:p.Glu109Val
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NM_001282618.1:c.239A>T
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NP_001269547.1:p.Glu80Val
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NM_001282619.1:c.434A>T
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NP_001269548.1:p.Glu145Val
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NM_001282620.1:c.434A>T
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NP_001269549.1:p.Glu145Val
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NM_002070.3:c.482A>T
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NP_002061.1:p.Glu161Val
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NM_002070.4:c.482A>T
MANE Select
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NP_002061.1:p.Glu161Val
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NM_001166425.2:c.371A>T
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NP_001159897.1:p.Glu124Val
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NM_001282618.2:c.239A>T
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NP_001269547.1:p.Glu80Val
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NM_001282619.2:c.434A>T
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NP_001269548.1:p.Glu145Val
|
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NM_001282620.2:c.434A>T
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NP_001269549.1:p.Glu145Val
|
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NM_001282617.2:c.326A>T
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NP_001269546.1:p.Glu109Val
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