ENST00000225964.10:c.1742G>C
MANE Select
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ENSP00000225964.6:p.Gly581Ala
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ENST00000225964.9:c.1742G>C
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ENSP00000225964.5:p.Gly581Ala
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ENST00000463440.1:n.132G>C
|
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ENST00000471344.1:n.774G>C
|
|
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ENST00000476387.1:n.91G>C
|
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NM_000088.3:c.1742G>C , LRG_1t1:c.1742G>C
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NP_000079.2:p.Gly581Ala
|
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XM_005257058.3:c.1742G>C
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XP_005257115.2:p.Gly581Ala
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XM_005257059.3:c.958-1275G>C
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XP_005257116.2:n.958-1275G>C
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XM_011524341.1:c.1544G>C
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XP_011522643.1:p.Gly515Ala
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XM_005257058.4:c.1742G>C
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XP_005257115.2:p.Gly581Ala
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XM_005257059.4:c.958-1275G>C
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XP_005257116.2:n.958-1275G>C
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NM_000088.4:c.1742G>C
MANE Select
|
NP_000079.2:p.Gly581Ala
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