ENST00000541682.7:c.330C>T
MANE Select
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ENSP00000446205.2:p.Ala110=
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ENST00000317814.8:c.315C>T
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ENSP00000314774.4:p.Ala105=
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|
ENST00000541682.6:c.330C>T
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ENSP00000446205.2:p.Ala110=
|
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ENST00000577735.1:c.306C>T
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ENSP00000462491.1:p.Ala102=
|
|
NM_001165967.1:c.330C>T
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NP_001159439.1:p.Ala110=
|
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NM_032580.3:c.315C>T
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NP_115969.2:p.Ala105=
|
|
XM_011524038.1:c.435C>T
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XP_011522340.1:p.Ala145=
|
|
XM_011524039.1:c.426C>T
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XP_011522341.1:p.Ala142=
|
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XM_011524040.1:c.426C>T
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XP_011522342.1:p.Ala142=
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|
XM_011524041.1:c.417C>T
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XP_011522343.1:p.Ala139=
|
|
XM_011524042.1:c.288C>T
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XP_011522344.1:p.Ala96=
|
|
XR_934203.1:n.69+2120G>A
|
|
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XM_017025232.1:c.435C>T
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XP_016880721.1:p.Ala145=
|
|
XM_024451007.1:c.435C>T
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XP_024306775.1:p.Ala145=
|
|
NM_001165967.2:c.330C>T
MANE Select
|
NP_001159439.1:p.Ala110=
|
|
NM_032580.4:c.315C>T
|
NP_115969.2:p.Ala105=
|
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