ENST00000295897.9:c.249T>A
MANE Select
|
ENSP00000295897.4:p.Ala83=
|
|
ENST00000295897.8:c.249T>A
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ENSP00000295897.4:p.Ala83=
|
|
ENST00000401494.7:c.137+1567T>A
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ENSP00000384695.3:n.137+1567T>A
|
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ENST00000415165.6:c.137+1567T>A
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ENSP00000401820.2:n.137+1567T>A
|
|
ENST00000441319.5:c.255T>A
|
ENSP00000392541.1:p.Ala85=
|
|
ENST00000476441.6:c.79+2334T>A
|
ENSP00000423727.1:n.79+2334T>A
|
|
ENST00000503124.5:c.11T>A
|
ENSP00000421027.1:p.Leu4Gln
|
|
ENST00000509063.5:c.249T>A
|
ENSP00000422784.1:p.Ala83=
|
|
ENST00000510166.5:n.285T>A
|
|
|
ENST00000514786.1:n.218T>A
|
|
|
ENST00000515133.5:n.290T>A
|
|
|
ENST00000621085.4:c.249T>A
|
ENSP00000483421.1:p.Ala83=
|
|
ENST00000621628.4:c.249T>A
|
ENSP00000480485.1:p.Ala83=
|
|
NM_000477.5:c.249T>A
|
NP_000468.1:p.Ala83=
|
|
NM_000477.6:c.249T>A
|
NP_000468.1:p.Ala83=
|
|
NM_000477.7:c.249T>A
MANE Select
|
NP_000468.1:p.Ala83=
|
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