ENST00000541682.7:c.681A=
MANE Select
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ENSP00000446205.2:p.Arg227=
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ENST00000317814.8:c.666A=
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ENSP00000314774.4:p.Arg222=
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ENST00000541682.6:c.681A=
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ENSP00000446205.2:p.Arg227=
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NM_001165967.1:c.681A=
|
NP_001159439.1:p.Arg227=
|
|
NM_032580.3:c.666A=
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NP_115969.2:p.Arg222=
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XM_011524038.1:c.786A=
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XP_011522340.1:p.Arg262=
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XM_011524039.1:c.777A=
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XP_011522341.1:p.Arg259=
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XM_011524040.1:c.777A=
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XP_011522342.1:p.Arg259=
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XM_011524041.1:c.768A=
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XP_011522343.1:p.Arg256=
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XM_011524042.1:c.639A=
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XP_011522344.1:p.Arg213=
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XR_934203.1:n.69+1769T=
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|
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XM_017025232.1:c.786A=
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XP_016880721.1:p.Arg262=
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XM_024451007.1:c.786A=
|
XP_024306775.1:p.Arg262=
|
|
NM_001165967.2:c.681A=
MANE Select
|
NP_001159439.1:p.Arg227=
|
|
NM_032580.4:c.666A=
|
NP_115969.2:p.Arg222=
|
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