ENST00000322344.8:c.1124G=
MANE Select
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ENSP00000323511.2:p.Gly375=
|
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ENST00000322344.7:c.1124G=
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ENSP00000323511.2:p.Gly375=
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|
ENST00000593706.3:n.479G=
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|
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ENST00000593946.5:c.*1051G=
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ENSP00000468896.1:n.*1051G=
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ENST00000594661.5:n.1625G=
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|
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ENST00000596014.5:c.1124G=
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ENSP00000472300.1:p.Gly375=
|
|
ENST00000600573.5:c.1031G=
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ENSP00000469826.1:p.Gly344=
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|
ENST00000600910.5:c.1124G=
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ENSP00000473137.1:p.Gly375=
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ENST00000601816.3:n.23G=
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|
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ENST00000625216.2:c.208-82G=
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ENSP00000486898.1:n.208-82G=
|
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ENST00000627232.2:c.1044G=
|
ENSP00000486037.1:n.1044G=
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|
ENST00000627317.1:c.745G=
|
|
|
ENST00000631020.2:c.1016G=
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ENSP00000486707.1:p.Gly339=
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NM_007254.3:c.1124G=
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NP_009185.2:p.Gly375=
|
|
NM_007254.4:c.1124G=
MANE Select
|
NP_009185.2:p.Gly375=
|
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