ENST00000205402.10:c.56G>A
MANE Select
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ENSP00000205402.3:p.Arg19Gln
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ENST00000639772.1:c.56G>A
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ENSP00000492159.1:p.Arg19Gln
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ENST00000205402.9:c.56G>A
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ENSP00000205402.3:p.Arg19Gln
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ENST00000415325.5:c.56G>A
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ENSP00000402593.1:p.Arg19Gln
|
|
ENST00000417551.5:c.56G>A
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ENSP00000390667.1:p.Arg19Gln
|
|
ENST00000437604.6:c.56G>A
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ENSP00000387542.2:p.Arg19Gln
|
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ENST00000440410.5:c.56G>A
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ENSP00000417016.1:p.Arg19Gln
|
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ENST00000450038.5:c.56G>A
|
ENSP00000409590.1:p.Arg19Gln
|
|
ENST00000451081.5:c.56G>A
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ENSP00000388077.1:p.Arg19Gln
|
|
ENST00000453354.5:n.121G>A
|
|
|
ENST00000460577.5:n.90G>A
|
|
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ENST00000485066.1:n.145G>A
|
|
|
ENST00000494441.1:n.201G>A
|
|
|
NM_000108.4:c.56G>A
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NP_000099.2:p.Arg19Gln
|
|
NM_001289750.1:c.-93G>A
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NP_001276679.1:n.-93G>A
|
|
NM_001289751.1:c.56G>A
|
NP_001276680.1:p.Arg19Gln
|
|
NM_001289752.1:c.56G>A
|
NP_001276681.1:p.Arg19Gln
|
|
NM_000108.5:c.56G>A
MANE Select
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NP_000099.2:p.Arg19Gln
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