ENST00000225964.10:c.2362G>A
MANE Select
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ENSP00000225964.6:p.Gly788Ser
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ENST00000225964.9:c.2362G>A
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ENSP00000225964.5:p.Gly788Ser
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ENST00000494334.1:n.127G>A
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|
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NM_000088.3:c.2362G>A , LRG_1t1:c.2362G>A
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NP_000079.2:p.Gly788Ser
|
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XM_005257058.3:c.2362G>A
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XP_005257115.2:p.Gly788Ser
|
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XM_005257059.3:c.1444G>A
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XP_005257116.2:p.Gly482Ser
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XM_011524341.1:c.2164G>A
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XP_011522643.1:p.Gly722Ser
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XM_005257058.4:c.2362G>A
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XP_005257115.2:p.Gly788Ser
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XM_005257059.4:c.1444G>A
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XP_005257116.2:p.Gly482Ser
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NM_000088.4:c.2362G>A
MANE Select
|
NP_000079.2:p.Gly788Ser
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