ENST00000392666.6:c.444A>T
MANE Select
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ENSP00000376434.1:p.Gly148=
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ENST00000324036.7:c.444A>T
|
ENSP00000316233.3:p.Gly148=
|
|
ENST00000392664.2:c.501A>T
|
ENSP00000376432.2:p.Gly167=
|
|
ENST00000392665.6:c.444A>T
|
ENSP00000376433.2:p.Gly148=
|
|
ENST00000392666.5:c.444A>T
|
ENSP00000376434.1:p.Gly148=
|
|
ENST00000440599.6:c.444A>T
|
ENSP00000406320.2:p.Gly148=
|
|
NM_000220.4:c.501A>T
|
NP_000211.1:p.Gly167=
|
|
NM_153764.2:c.444A>T
|
NP_722448.1:p.Gly148=
|
|
NM_153765.2:c.495A>T
|
NP_722449.3:p.Gly165=
|
|
NM_153766.2:c.444A>T
|
NP_722450.1:p.Gly148=
|
|
NM_153767.3:c.444A>T
|
NP_722451.1:p.Gly148=
|
|
NM_000220.6:c.501A>T
|
NP_000211.1:p.Gly167=
|
|
NM_153764.3:c.444A>T
|
NP_722448.1:p.Gly148=
|
|
NM_153765.3:c.495A>T
|
NP_722449.3:p.Gly165=
|
|
NM_153766.3:c.444A>T
MANE Select
|
NP_722450.1:p.Gly148=
|
|
NM_153767.4:c.444A>T
|
NP_722451.1:p.Gly148=
|
|