ENST00000356141.9:c.1776G>C
MANE Select
|
ENSP00000348460.4:p.Gln592His
|
|
ENST00000551634.6:c.1785G>C
|
ENSP00000448373.2:p.Gln595His
|
|
ENST00000680362.1:c.1676G>C
|
|
|
ENST00000681323.1:c.793+2502G>C
|
|
|
ENST00000346562.6:c.1680G>C
|
ENSP00000319610.5:p.Gln560His
|
|
ENST00000356141.8:c.1776G>C
|
ENSP00000348460.4:p.Gln592His
|
|
ENST00000357798.9:c.1737G>C
|
ENSP00000350446.5:p.Gln579His
|
|
ENST00000548645.5:c.1686G>C
|
ENSP00000448916.1:p.Gln562His
|
|
ENST00000551492.5:c.1791G>C
|
ENSP00000450392.1:p.Gln597His
|
|
ENST00000551634.5:c.1698G>C
|
ENSP00000448373.1:p.Gln566His
|
|
NM_001164749.1:c.1776G>C
|
NP_001158221.1:p.Gln592His
|
|
NM_001165893.1:c.1686G>C
|
NP_001159365.1:p.Gln562His
|
|
NM_022123.2:c.1680G>C
|
NP_071406.1:p.Gln560His
|
|
NM_173159.2:c.1737G>C
|
NP_775182.1:p.Gln579His
|
|
XM_005267991.2:c.1797G>C
|
XP_005268048.1:p.Gln599His
|
|
XM_005267992.2:c.1791G>C
|
XP_005268049.1:p.Gln597His
|
|
XM_005267993.2:c.1737G>C
|
XP_005268050.1:p.Gln579His
|
|
XM_011537067.1:c.1827G>C
|
XP_011535369.1:p.Gln609His
|
|
XM_011537068.1:c.1818G>C
|
XP_011535370.1:p.Gln606His
|
|
XM_011537069.1:c.1788G>C
|
XP_011535371.1:p.Gln596His
|
|
XM_011537070.1:c.1731G>C
|
XP_011535372.1:p.Gln577His
|
|
XM_011537071.1:c.1698G>C
|
XP_011535373.1:p.Gln566His
|
|
XM_011537072.1:c.1677G>C
|
XP_011535374.1:p.Gln559His
|
|
XM_011537073.1:c.1470G>C
|
XP_011535375.1:p.Gln490His
|
|
XM_011537074.1:c.1470G>C
|
XP_011535376.1:p.Gln490His
|
|
XM_005267991.3:c.1884G>C
|
XP_005268048.2:p.Gln628His
|
|
XM_005267992.3:c.1878G>C
|
XP_005268049.2:p.Gln626His
|
|
XM_011537067.2:c.1827G>C
|
XP_011535369.1:p.Gln609His
|
|
XM_011537069.2:c.1875G>C
|
XP_011535371.2:p.Gln625His
|
|
XM_011537070.2:c.1731G>C
|
XP_011535372.1:p.Gln577His
|
|
XM_011537071.2:c.1785G>C
|
XP_011535373.2:p.Gln595His
|
|
XM_011537072.2:c.1677G>C
|
XP_011535374.1:p.Gln559His
|
|
XM_017021582.1:c.1935G>C
|
XP_016877071.1:p.Gln645His
|
|
XM_017021583.1:c.1926G>C
|
XP_016877072.1:p.Gln642His
|
|
XM_017021584.1:c.1845G>C
|
XP_016877073.1:p.Gln615His
|
|
XM_017021585.1:c.1794G>C
|
XP_016877074.1:p.Gln598His
|
|
XM_017021586.1:c.1470G>C
|
XP_016877075.1:p.Gln490His
|
|
XM_017021587.1:c.1470G>C
|
XP_016877076.1:p.Gln490His
|
|
XM_017021588.1:c.1470G>C
|
XP_016877077.1:p.Gln490His
|
|
NM_001164749.2:c.1776G>C
MANE Select
|
NP_001158221.1:p.Gln592His
|
|
NM_001165893.2:c.1686G>C
|
NP_001159365.1:p.Gln562His
|
|
NM_022123.3:c.1680G>C
|
NP_071406.1:p.Gln560His
|
|
NM_173159.3:c.1737G>C
|
NP_775182.1:p.Gln579His
|
|
NM_001394988.1:c.1731G>C
|
NP_001381917.1:p.Gln577His
|
|
NM_001394989.1:c.1677G>C
|
NP_001381918.1:p.Gln559His
|
|