ENST00000305046.13:c.126G>A
MANE Select
|
ENSP00000306606.8:p.Val42=
|
|
ENST00000639454.1:c.126G>A
|
ENSP00000491622.1:p.Val42=
|
|
ENST00000305046.12:c.126G>A
|
ENSP00000306606.8:p.Val42=
|
|
ENST00000504498.1:n.180G>A
|
|
|
ENST00000506651.5:c.6G>A
|
ENSP00000425998.2:p.Val2=
|
|
ENST00000515694.4:n.2221G>A
|
|
|
ENST00000625860.2:c.6G>A
|
ENSP00000486614.1:p.Val2=
|
|
ENST00000632775.1:n.689G>A
|
|
|
NM_000668.5:c.126G>A
|
NP_000659.2:p.Val42=
|
|
NM_001286650.1:c.6G>A
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NP_001273579.1:p.Val2=
|
|
NM_000668.6:c.126G>A
MANE Select
|
NP_000659.2:p.Val42=
|
|
NM_001286650.2:c.6G>A
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NP_001273579.1:p.Val2=
|
|