ENST00000691183.1:c.*576G=
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ENSP00000509954.1:n.*576G=
|
|
ENST00000378842.8:c.988G=
MANE Select
|
ENSP00000368119.4:p.Ala330=
|
|
ENST00000378842.7:c.988G=
|
ENSP00000368119.3:p.Ala330=
|
|
ENST00000450095.6:c.661G=
|
ENSP00000401956.2:p.Ala221=
|
|
ENST00000488412.2:n.572G=
|
|
|
ENST00000489643.6:n.1396G=
|
|
|
ENST00000554550.5:c.*608G=
|
ENSP00000451435.1:n.*608G=
|
|
ENST00000554638.5:n.1460G=
|
|
|
ENST00000555020.5:n.1777G=
|
|
|
ENST00000555754.1:n.436G=
|
|
|
ENST00000556278.1:c.432+1037G=
|
ENSP00000451792.1:n.432+1037G=
|
|
ENST00000557706.5:n.1563G=
|
|
|
NM_000155.3:c.988G=
|
NP_000146.2:p.Ala330=
|
|
NM_001258332.1:c.661G=
|
NP_001245261.1:p.Ala221=
|
|
NM_000155.4:c.988G=
MANE Select
|
NP_000146.2:p.Ala330=
|
|
NM_001258332.2:c.661G=
|
NP_001245261.1:p.Ala221=
|
|