NM_000093.5:c.4906G=
MANE Select
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NP_000084.3:p.Ala1636=
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ENST00000371817.8:c.4906G=
MANE Select
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ENSP00000360882.3:p.Ala1636=
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NM_000093.4:c.4906G=
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NP_000084.3:p.Ala1636=
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NM_001278074.1:c.4906G=
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NP_001265003.1:p.Ala1636=
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NR_103451.2:n.71-4598C=
|
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ENST00000371817.7:c.4906G=
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ENSP00000360882.3:p.Ala1636=
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ENST00000371820.3:c.164G=
|
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ENST00000371820.4:c.4906G=
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ENSP00000360885.4:p.Ala1636=
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ENST00000460264.5:n.374G=
|
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ENST00000465877.1:n.86G=
|
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ENST00000618395.4:c.4906G=
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ENSP00000481360.1:p.Ala1636=
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XM_017014266.2:c.4906G=
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XP_016869755.1:p.Ala1636=
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XR_001746183.1:n.5304G=
|
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XR_929712.1:n.5308G=
|
|
XR_929713.1:n.5308G=
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