ENST00000225964.10:c.1905C>G
MANE Select
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ENSP00000225964.6:p.Gly635=
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ENST00000225964.9:c.1905C>G
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ENSP00000225964.5:p.Gly635=
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ENST00000476387.1:n.254C>G
|
|
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NM_000088.3:c.1905C>G , LRG_1t1:c.1905C>G
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NP_000079.2:p.Gly635=
|
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XM_005257058.3:c.1905C>G
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XP_005257115.2:p.Gly635=
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XM_005257059.3:c.987C>G
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XP_005257116.2:p.Gly329=
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XM_011524341.1:c.1707C>G
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XP_011522643.1:p.Gly569=
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XM_005257058.4:c.1905C>G
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XP_005257115.2:p.Gly635=
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XM_005257059.4:c.987C>G
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XP_005257116.2:p.Gly329=
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NM_000088.4:c.1905C>G
MANE Select
|
NP_000079.2:p.Gly635=
|
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