ENST00000684241.1:n.1159T=
|
|
|
ENST00000262186.10:c.326T=
MANE Select
|
ENSP00000262186.5:p.Leu109=
|
|
ENST00000262186.9:c.326T=
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ENSP00000262186.5:p.Leu109=
|
|
ENST00000430723.4:c.149T=
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ENSP00000387657.4:p.Leu50=
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|
ENST00000532957.5:n.549T=
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NM_000238.3:c.326T= , LRG_288t1:c.326T=
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NP_000229.1:p.Leu109=
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|
NM_172056.2:c.326T= , LRG_288t2:c.326T=
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NP_742053.1:p.Leu109=
|
|
XM_011516185.1:c.26T=
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XP_011514487.1:p.Leu9=
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|
XM_011516186.1:c.326T=
|
XP_011514488.1:p.Leu109=
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|
XM_011516185.2:c.26T=
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XP_011514487.1:p.Leu9=
|
|
XM_011516186.3:c.326T=
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XP_011514488.1:p.Leu109=
|
|
XM_017012195.1:c.176T=
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XP_016867684.1:p.Leu59=
|
|
XM_017012196.1:c.149T=
|
XP_016867685.1:p.Leu50=
|
|
NM_000238.4:c.326T=
MANE Select
|
NP_000229.1:p.Leu109=
|
|