ENST00000282058.11:c.779G>A
MANE Select
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ENSP00000282058.5:p.Arg260Gln
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|
ENST00000282058.10:c.779G>A
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ENSP00000282058.5:p.Arg260Gln
|
|
ENST00000585518.5:c.*12G>A
|
ENSP00000467975.1:n.*12G>A
|
|
ENST00000586060.5:c.*157G>A
|
ENSP00000466364.1:n.*157G>A
|
|
ENST00000588704.1:n.735G>A
|
|
|
ENST00000589554.5:c.*223G>A
|
ENSP00000466715.1:n.*223G>A
|
|
ENST00000591715.5:c.*576G>A
|
ENSP00000465093.1:n.*576G>A
|
|
ENST00000593165.5:c.907G>A
|
|
|
ENST00000595199.1:n.225G>A
|
|
|
NM_138443.3:c.779G>A
|
NP_612452.1:p.Arg260Gln
|
|
NR_026978.1:n.899G>A
|
|
|
NM_138443.4:c.779G>A
MANE Select
|
NP_612452.1:p.Arg260Gln
|
|
NR_026978.2:n.846G>A
|
|
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