ENST00000684241.1:n.1775C=
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|
|
ENST00000262186.10:c.942C=
MANE Select
|
ENSP00000262186.5:p.Gly314=
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|
ENST00000262186.9:c.942C=
|
ENSP00000262186.5:p.Gly314=
|
|
ENST00000430723.4:c.594C=
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ENSP00000387657.4:p.Gly198=
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|
ENST00000532957.5:n.1165C=
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NM_000238.3:c.942C= , LRG_288t1:c.942C=
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NP_000229.1:p.Gly314=
|
|
NM_172056.2:c.942C= , LRG_288t2:c.942C=
|
NP_742053.1:p.Gly314=
|
|
XM_011516185.1:c.642C=
|
XP_011514487.1:p.Gly214=
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|
XM_011516186.1:c.942C=
|
XP_011514488.1:p.Gly314=
|
|
XM_011516185.2:c.642C=
|
XP_011514487.1:p.Gly214=
|
|
XM_011516186.3:c.942C=
|
XP_011514488.1:p.Gly314=
|
|
XM_017012195.1:c.792C=
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XP_016867684.1:p.Gly264=
|
|
XM_017012196.1:c.765C=
|
XP_016867685.1:p.Gly255=
|
|
NM_000238.4:c.942C=
MANE Select
|
NP_000229.1:p.Gly314=
|
|