ENST00000356839.10:c.822C>T
MANE Select
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ENSP00000349297.5:p.Ala274=
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ENST00000322910.9:c.*777C>T
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ENSP00000325395.5:n.*777C>T
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ENST00000350303.9:c.756C>T
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ENSP00000344152.5:p.Ala252=
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ENST00000356839.9:c.822C>T
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ENSP00000349297.5:p.Ala274=
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ENST00000543245.6:c.891C>T
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ENSP00000438689.2:p.Ala297=
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ENST00000577191.5:n.994C>T
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ENST00000581378.5:c.540C>T
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ENST00000582379.1:n.206C>T
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NM_000018.3:c.822C>T
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NP_000009.1:p.Ala274=
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NM_001033859.2:c.756C>T
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NP_001029031.1:p.Ala252=
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NM_001270447.1:c.891C>T
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NP_001257376.1:p.Ala297=
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NM_001270448.1:c.594C>T
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NP_001257377.1:p.Ala198=
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XM_006721516.2:c.822C>T
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XP_006721579.2:p.Ala274=
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XM_011523829.1:c.822C>T
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XP_011522131.1:p.Ala274=
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XM_011523830.1:c.822C>T
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XP_011522132.1:p.Ala274=
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XR_934021.1:n.929C>T
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XR_934022.1:n.929C>T
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XR_934023.1:n.929C>T
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XM_006721516.3:c.822C>T
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XP_006721579.2:p.Ala274=
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XM_011523829.2:c.822C>T
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XP_011522131.1:p.Ala274=
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XM_011523830.2:c.822C>T
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XP_011522132.1:p.Ala274=
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XM_024450741.1:c.822C>T
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XP_024306509.1:p.Ala274=
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XR_934021.2:n.881C>T
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XR_934022.2:n.881C>T
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XR_934023.2:n.881C>T
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NM_000018.4:c.822C>T
MANE Select
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NP_000009.1:p.Ala274=
|
|
NM_001033859.3:c.756C>T
|
NP_001029031.1:p.Ala252=
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|
NM_001270447.2:c.891C>T
|
NP_001257376.1:p.Ala297=
|
|
NM_001270448.2:c.594C>T
|
NP_001257377.1:p.Ala198=
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