ENST00000684241.1:n.1261A>G
|
|
|
ENST00000262186.10:c.428A>G
MANE Select
|
ENSP00000262186.5:p.His143Arg
|
|
ENST00000262186.9:c.428A>G
|
ENSP00000262186.5:p.His143Arg
|
|
ENST00000430723.4:c.234+17A>G
|
ENSP00000387657.4:n.234+17A>G
|
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ENST00000532957.5:n.651A>G
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|
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NM_000238.3:c.428A>G , LRG_288t1:c.428A>G
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NP_000229.1:p.His143Arg
|
|
NM_172056.2:c.428A>G , LRG_288t2:c.428A>G
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NP_742053.1:p.His143Arg
|
|
XM_011516185.1:c.128A>G
|
XP_011514487.1:p.His43Arg
|
|
XM_011516186.1:c.428A>G
|
XP_011514488.1:p.His143Arg
|
|
XM_011516185.2:c.128A>G
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XP_011514487.1:p.His43Arg
|
|
XM_011516186.3:c.428A>G
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XP_011514488.1:p.His143Arg
|
|
XM_017012195.1:c.278A>G
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XP_016867684.1:p.His93Arg
|
|
XM_017012196.1:c.251A>G
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XP_016867685.1:p.His84Arg
|
|
NM_000238.4:c.428A>G
MANE Select
|
NP_000229.1:p.His143Arg
|
|