ENST00000684241.1:n.3941C>G
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ENST00000262186.10:c.3108C>G
MANE Select
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ENSP00000262186.5:p.Gly1036=
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ENST00000330883.9:c.2088C>G
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ENSP00000328531.4:p.Gly696=
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ENST00000262186.9:c.3108C>G
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ENSP00000262186.5:p.Gly1036=
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ENST00000330883.8:c.2088C>G
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ENSP00000328531.4:p.Gly696=
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NM_000238.3:c.3108C>G , LRG_288t1:c.3108C>G
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NP_000229.1:p.Gly1036=
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NM_172057.2:c.2088C>G , LRG_288t3:c.2088C>G
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NP_742054.1:p.Gly696=
|
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XM_011516185.1:c.2808C>G
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XP_011514487.1:p.Gly936=
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XM_011516185.2:c.2808C>G
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XP_011514487.1:p.Gly936=
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XM_017012195.1:c.2958C>G
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XP_016867684.1:p.Gly986=
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XM_017012196.1:c.2931C>G
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XP_016867685.1:p.Gly977=
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NM_000238.4:c.3108C>G
MANE Select
|
NP_000229.1:p.Gly1036=
|
|
NM_172057.3:c.2088C>G
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NP_742054.1:p.Gly696=
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