ENST00000376810.6:c.476A>G
MANE Select
|
ENSP00000366006.5:p.His159Arg
|
|
ENST00000376804.2:c.476A>G
|
ENSP00000366000.1:p.His159Arg
|
|
ENST00000376810.5:c.476A>G
|
ENSP00000366006.5:p.His159Arg
|
|
ENST00000483738.1:c.74A>G
|
ENSP00000473453.1:p.His25Arg
|
|
ENST00000486588.6:c.119A>G
|
ENSP00000473612.1:p.His40Arg
|
|
NM_013319.2:c.476A>G
|
NP_037451.1:p.His159Arg
|
|
XM_006710590.2:c.476A>G
|
XP_006710653.1:p.His159Arg
|
|
XM_011541304.1:c.476A>G
|
XP_011539606.1:p.His159Arg
|
|
XR_946616.1:n.810A>G
|
|
|
NM_001330349.1:c.476A>G
|
NP_001317278.1:p.His159Arg
|
|
NM_001330350.1:c.476A>G
|
NP_001317279.1:p.His159Arg
|
|
XR_946616.3:n.810A>G
|
|
|
NM_001330349.2:c.476A>G
|
NP_001317278.1:p.His159Arg
|
|
NM_001330350.2:c.476A>G
|
NP_001317279.1:p.His159Arg
|
|
NM_013319.3:c.476A>G
MANE Select
|
NP_037451.1:p.His159Arg
|
|