ENST00000700075.1:c.69C>G
|
ENSP00000514784.1:p.Val23=
|
|
ENST00000342771.10:c.2001C>G
MANE Select
|
ENSP00000344087.4:p.Val667=
|
|
ENST00000439256.2:c.99C>G
|
ENSP00000407058.2:p.Val33=
|
|
ENST00000443672.2:c.336C>G
|
ENSP00000393548.2:p.Val112=
|
|
ENST00000449547.6:c.94C>G
|
|
|
ENST00000464768.2:n.669C>G
|
|
|
ENST00000644359.1:c.582C>G
|
ENSP00000494561.1:p.Val194=
|
|
ENST00000644506.1:c.627C>G
|
ENSP00000496672.1:p.Val209=
|
|
ENST00000644939.1:c.1998C>G
|
ENSP00000496726.1:p.Val666=
|
|
ENST00000646136.1:n.312C>G
|
|
|
ENST00000647140.1:c.866C>G
|
|
|
ENST00000342771.8:c.2001C>G
|
ENSP00000344087.4:p.Val667=
|
|
ENST00000406775.6:c.1929C>G
|
ENSP00000385263.2:p.Val643=
|
|
ENST00000439256.1:c.99C>G
|
|
|
ENST00000464768.1:n.667C>G
|
|
|
ENST00000465899.1:n.498C>G
|
|
|
ENST00000498384.5:n.369C>G
|
|
|
ENST00000611706.4:c.1257C>G
|
ENSP00000478134.1:p.Val419=
|
|
ENST00000615871.4:c.1185C>G
|
ENSP00000479325.1:p.Val395=
|
|
NM_001127231.2:c.1929C>G
|
NP_001120703.1:p.Val643=
|
|
NM_015570.3:c.2001C>G
|
NP_056385.1:p.Val667=
|
|
XM_005250257.1:c.648C>G
|
XP_005250314.1:p.Val216=
|
|
XM_011516010.1:c.2022C>G
|
XP_011514312.1:p.Val674=
|
|
XM_011516011.1:c.2019C>G
|
XP_011514313.1:p.Val673=
|
|
XM_011516012.1:c.1956C>G
|
XP_011514314.1:p.Val652=
|
|
XM_011516013.1:c.1950C>G
|
XP_011514315.1:p.Val650=
|
|
XM_011516014.1:c.1920C>G
|
XP_011514316.1:p.Val640=
|
|
XM_011516015.1:c.1758C>G
|
XP_011514317.1:p.Val586=
|
|
XM_011516016.1:c.1731C>G
|
XP_011514318.1:p.Val577=
|
|
XM_011516017.1:c.1548C>G
|
XP_011514319.1:p.Val516=
|
|
XM_011516018.1:c.1521C>G
|
XP_011514320.1:p.Val507=
|
|
XM_005250257.2:c.648C>G
|
XP_005250314.1:p.Val216=
|
|
XM_011516010.2:c.2022C>G
|
XP_011514312.1:p.Val674=
|
|
XM_011516011.2:c.2019C>G
|
XP_011514313.1:p.Val673=
|
|
XM_011516012.2:c.1956C>G
|
XP_011514314.1:p.Val652=
|
|
XM_011516013.2:c.1950C>G
|
XP_011514315.1:p.Val650=
|
|
XM_011516014.2:c.1920C>G
|
XP_011514316.1:p.Val640=
|
|
XM_011516017.2:c.1548C>G
|
XP_011514319.1:p.Val516=
|
|
XM_011516018.2:c.1521C>G
|
XP_011514320.1:p.Val507=
|
|
XM_017011951.2:c.2022C>G
|
XP_016867440.1:p.Val674=
|
|
NM_001127231.3:c.1929C>G
|
NP_001120703.1:p.Val643=
|
|
NM_015570.4:c.2001C>G
MANE Select
|
NP_056385.1:p.Val667=
|
|