ENST00000691183.1:c.*461G>T
|
ENSP00000509954.1:n.*461G>T
|
|
ENST00000378842.8:c.873G>T
MANE Select
|
ENSP00000368119.4:p.Glu291Asp
|
|
ENST00000378842.7:c.873G>T
|
ENSP00000368119.3:p.Glu291Asp
|
|
ENST00000450095.6:c.546G>T
|
ENSP00000401956.2:p.Glu182Asp
|
|
ENST00000488412.2:n.129G>T
|
|
|
ENST00000489643.6:n.953G>T
|
|
|
ENST00000554550.5:c.*493G>T
|
ENSP00000451435.1:n.*493G>T
|
|
ENST00000554638.5:n.1345G>T
|
|
|
ENST00000555020.5:n.1334G>T
|
|
|
ENST00000555086.5:n.980G>T
|
|
|
ENST00000555754.1:n.321G>T
|
|
|
ENST00000556278.1:c.432+594G>T
|
ENSP00000451792.1:n.432+594G>T
|
|
ENST00000557706.5:n.1448G>T
|
|
|
NM_000155.3:c.873G>T
|
NP_000146.2:p.Glu291Asp
|
|
NM_001258332.1:c.546G>T
|
NP_001245261.1:p.Glu182Asp
|
|
NM_000155.4:c.873G>T
MANE Select
|
NP_000146.2:p.Glu291Asp
|
|
NM_001258332.2:c.546G>T
|
NP_001245261.1:p.Glu182Asp
|
|