ENST00000684241.1:n.1939A>C
|
|
|
ENST00000262186.10:c.1106A>C
MANE Select
|
ENSP00000262186.5:p.Asn369Thr
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|
ENST00000262186.9:c.1106A>C
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ENSP00000262186.5:p.Asn369Thr
|
|
ENST00000430723.4:c.758A>C
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ENSP00000387657.4:p.Asn253Thr
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ENST00000532957.5:n.1329A>C
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|
|
NM_000238.3:c.1106A>C , LRG_288t1:c.1106A>C
|
NP_000229.1:p.Asn369Thr
|
|
NM_172056.2:c.1106A>C , LRG_288t2:c.1106A>C
|
NP_742053.1:p.Asn369Thr
|
|
XM_011516185.1:c.806A>C
|
XP_011514487.1:p.Asn269Thr
|
|
XM_011516186.1:c.1106A>C
|
XP_011514488.1:p.Asn369Thr
|
|
XM_011516185.2:c.806A>C
|
XP_011514487.1:p.Asn269Thr
|
|
XM_011516186.3:c.1106A>C
|
XP_011514488.1:p.Asn369Thr
|
|
XM_017012195.1:c.956A>C
|
XP_016867684.1:p.Asn319Thr
|
|
XM_017012196.1:c.929A>C
|
XP_016867685.1:p.Asn310Thr
|
|
NM_000238.4:c.1106A>C
MANE Select
|
NP_000229.1:p.Asn369Thr
|
|