ENST00000683044.1:c.*1138C>A
|
ENSP00000507095.1:n.*1138C>A
|
|
ENST00000683288.1:c.*2066C>A
|
ENSP00000507477.1:n.*2066C>A
|
|
ENST00000683748.1:c.2094C>A
|
ENSP00000507377.1:p.Gly698=
|
|
ENST00000683905.1:c.*743C>A
|
ENSP00000506960.1:n.*743C>A
|
|
ENST00000684139.1:c.1602C>A
|
ENSP00000507295.1:p.Gly534=
|
|
ENST00000684210.1:n.1780C>A
|
|
|
ENST00000684314.1:c.1962C>A
|
ENSP00000507700.1:p.Gly654=
|
|
ENST00000684331.1:c.*787C>A
|
ENSP00000507431.1:n.*787C>A
|
|
ENST00000684463.1:n.705C>A
|
|
|
ENST00000684646.1:c.1854C>A
|
ENSP00000507723.1:p.Gly618=
|
|
ENST00000309971.9:c.2067C>A
MANE Select
|
ENSP00000308622.5:p.Gly689=
|
|
ENST00000309971.8:c.2067C>A
|
ENSP00000308622.4:p.Gly689=
|
|
NM_001003722.1:c.2067C>A , LRG_484t1:c.2067C>A
|
NP_001003722.1:p.Gly689=
|
|
XM_006717059.2:c.2103C>A
|
XP_006717122.1:p.Gly701=
|
|
XM_006717060.2:c.2076C>A
|
XP_006717123.1:p.Gly692=
|
|
XM_011518549.1:c.2103C>A
|
XP_011516851.1:p.Gly701=
|
|
XM_011518550.1:c.2103C>A
|
XP_011516852.1:p.Gly701=
|
|
XM_011518551.1:c.2094C>A
|
XP_011516853.1:p.Gly698=
|
|
XM_011518552.1:c.1344C>A
|
XP_011516854.1:p.Gly448=
|
|
XR_242681.3:n.100+2239G>T
|
|
|
XM_006717059.3:c.2103C>A
|
XP_006717122.1:p.Gly701=
|
|
XM_006717060.3:c.2076C>A
|
XP_006717123.1:p.Gly692=
|
|
XM_011518551.2:c.2094C>A
|
XP_011516853.1:p.Gly698=
|
|
XM_024447519.1:c.2076C>A
|
XP_024303287.1:p.Gly692=
|
|
NM_001003722.2:c.2067C>A
MANE Select
|
NP_001003722.1:p.Gly689=
|
|