ENST00000461280.2:n.1110C>G
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|
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ENST00000684241.1:n.2645C>G
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|
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ENST00000262186.10:c.1812C>G
MANE Select
|
ENSP00000262186.5:p.Gly604=
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ENST00000330883.9:c.792C>G
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ENSP00000328531.4:p.Gly264=
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|
ENST00000262186.9:c.1812C>G
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ENSP00000262186.5:p.Gly604=
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|
ENST00000330883.8:c.792C>G
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ENSP00000328531.4:p.Gly264=
|
|
ENST00000430723.4:c.1464C>G
|
ENSP00000387657.4:p.Gly488=
|
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ENST00000461280.1:n.1099C>G
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|
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ENST00000473610.5:n.1117C>G
|
|
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ENST00000532957.5:n.2035C>G
|
|
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NM_000238.3:c.1812C>G , LRG_288t1:c.1812C>G
|
NP_000229.1:p.Gly604=
|
|
NM_001204798.1:c.792C>G
|
NP_001191727.1:p.Gly264=
|
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NM_172056.2:c.1812C>G , LRG_288t2:c.1812C>G
|
NP_742053.1:p.Gly604=
|
|
NM_172057.2:c.792C>G , LRG_288t3:c.792C>G
|
NP_742054.1:p.Gly264=
|
|
XM_011516185.1:c.1512C>G
|
XP_011514487.1:p.Gly504=
|
|
XM_011516186.1:c.1812C>G
|
XP_011514488.1:p.Gly604=
|
|
XM_011516185.2:c.1512C>G
|
XP_011514487.1:p.Gly504=
|
|
XM_011516186.3:c.1812C>G
|
XP_011514488.1:p.Gly604=
|
|
XM_017012195.1:c.1662C>G
|
XP_016867684.1:p.Gly554=
|
|
XM_017012196.1:c.1635C>G
|
XP_016867685.1:p.Gly545=
|
|
NM_000238.4:c.1812C>G
MANE Select
|
NP_000229.1:p.Gly604=
|
|
NM_001204798.2:c.792C>G
|
NP_001191727.1:p.Gly264=
|
|
NM_172057.3:c.792C>G
|
NP_742054.1:p.Gly264=
|
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