ENST00000684241.1:n.1593C>G
|
|
|
ENST00000262186.10:c.760C>G
MANE Select
|
ENSP00000262186.5:p.His254Asp
|
|
ENST00000262186.9:c.760C>G
|
ENSP00000262186.5:p.His254Asp
|
|
ENST00000430723.4:c.412C>G
|
ENSP00000387657.4:p.His138Asp
|
|
ENST00000532957.5:n.983C>G
|
|
|
NM_000238.3:c.760C>G , LRG_288t1:c.760C>G
|
NP_000229.1:p.His254Asp
|
|
NM_172056.2:c.760C>G , LRG_288t2:c.760C>G
|
NP_742053.1:p.His254Asp
|
|
XM_011516185.1:c.460C>G
|
XP_011514487.1:p.His154Asp
|
|
XM_011516186.1:c.760C>G
|
XP_011514488.1:p.His254Asp
|
|
XM_011516185.2:c.460C>G
|
XP_011514487.1:p.His154Asp
|
|
XM_011516186.3:c.760C>G
|
XP_011514488.1:p.His254Asp
|
|
XM_017012195.1:c.610C>G
|
XP_016867684.1:p.His204Asp
|
|
XM_017012196.1:c.583C>G
|
XP_016867685.1:p.His195Asp
|
|
NM_000238.4:c.760C>G
MANE Select
|
NP_000229.1:p.His254Asp
|
|