ENST00000273064.11:c.422G>T
MANE Select
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ENSP00000273064.6:p.Gly141Val
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ENST00000273064.10:c.422G>T
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ENSP00000273064.6:p.Gly141Val
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ENST00000295701.9:c.422G>T
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ENSP00000295701.5:p.Gly141Val
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ENST00000542068.5:c.422G>T
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ENSP00000443687.1:p.Gly141Val
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ENST00000627282.2:c.422G>T
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ENSP00000486540.1:p.Gly141Val
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NM_001271634.1:c.422G>T
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NP_001258563.1:p.Gly141Val
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NM_001271635.1:c.422G>T
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NP_001258564.1:p.Gly141Val
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NM_005444.2:c.422G>T
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NP_005435.1:p.Gly141Val
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NR_073390.1:n.695+1627G>T
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XM_011512138.1:c.263G>T
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XP_011510440.1:p.Gly88Val
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XM_011512138.3:c.263G>T
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XP_011510440.1:p.Gly88Val
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XM_017005248.1:c.260G>T
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XP_016860737.1:p.Gly87Val
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XM_017005249.2:c.263G>T
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XP_016860738.1:p.Gly88Val
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NM_001271634.2:c.422G>T
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NP_001258563.1:p.Gly141Val
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NM_005444.3:c.422G>T
MANE Select
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NP_005435.1:p.Gly141Val
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NR_073390.2:n.436+1627G>T
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NM_001271635.2:c.422G>T
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NP_001258564.1:p.Gly141Val
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