ENST00000684241.1:n.1938A>C
|
|
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ENST00000262186.10:c.1105A>C
MANE Select
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ENSP00000262186.5:p.Asn369His
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|
ENST00000262186.9:c.1105A>C
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ENSP00000262186.5:p.Asn369His
|
|
ENST00000430723.4:c.757A>C
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ENSP00000387657.4:p.Asn253His
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ENST00000532957.5:n.1328A>C
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|
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NM_000238.3:c.1105A>C , LRG_288t1:c.1105A>C
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NP_000229.1:p.Asn369His
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NM_172056.2:c.1105A>C , LRG_288t2:c.1105A>C
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NP_742053.1:p.Asn369His
|
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XM_011516185.1:c.805A>C
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XP_011514487.1:p.Asn269His
|
|
XM_011516186.1:c.1105A>C
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XP_011514488.1:p.Asn369His
|
|
XM_011516185.2:c.805A>C
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XP_011514487.1:p.Asn269His
|
|
XM_011516186.3:c.1105A>C
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XP_011514488.1:p.Asn369His
|
|
XM_017012195.1:c.955A>C
|
XP_016867684.1:p.Asn319His
|
|
XM_017012196.1:c.928A>C
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XP_016867685.1:p.Asn310His
|
|
NM_000238.4:c.1105A>C
MANE Select
|
NP_000229.1:p.Asn369His
|
|