ENST00000684241.1:n.1799C=
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|
|
ENST00000262186.10:c.966C=
MANE Select
|
ENSP00000262186.5:p.Ser322=
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|
ENST00000262186.9:c.966C=
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ENSP00000262186.5:p.Ser322=
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|
ENST00000430723.4:c.618C=
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ENSP00000387657.4:p.Ser206=
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|
ENST00000532957.5:n.1189C=
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NM_000238.3:c.966C= , LRG_288t1:c.966C=
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NP_000229.1:p.Ser322=
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|
NM_172056.2:c.966C= , LRG_288t2:c.966C=
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NP_742053.1:p.Ser322=
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|
XM_011516185.1:c.666C=
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XP_011514487.1:p.Ser222=
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|
XM_011516186.1:c.966C=
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XP_011514488.1:p.Ser322=
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|
XM_011516185.2:c.666C=
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XP_011514487.1:p.Ser222=
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|
XM_011516186.3:c.966C=
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XP_011514488.1:p.Ser322=
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|
XM_017012195.1:c.816C=
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XP_016867684.1:p.Ser272=
|
|
XM_017012196.1:c.789C=
|
XP_016867685.1:p.Ser263=
|
|
NM_000238.4:c.966C=
MANE Select
|
NP_000229.1:p.Ser322=
|
|