ENST00000695651.1:n.2277G=
|
|
|
ENST00000695653.1:c.1838G=
|
ENSP00000512084.1:p.Arg613=
|
|
ENST00000695654.1:c.2954G=
|
ENSP00000512085.1:p.Arg985=
|
|
ENST00000695690.1:n.120G=
|
|
|
ENST00000695691.1:n.120G=
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|
|
ENST00000245907.11:c.3929G=
MANE Select
|
ENSP00000245907.4:p.Arg1310=
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|
ENST00000245907.10:c.3929G=
|
ENSP00000245907.4:p.Arg1310=
|
|
ENST00000596238.1:n.372G=
|
|
|
ENST00000596548.1:c.11G=
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ENSP00000469744.1:p.Arg4=
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|
ENST00000601008.1:c.241+1718G=
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ENSP00000471384.1:n.241+1718G=
|
|
NM_000064.3:c.3929G=
|
NP_000055.2:p.Arg1310=
|
|
NM_000064.4:c.3929G=
MANE Select
|
NP_000055.2:p.Arg1310=
|
|