ENST00000270301.12:c.3226G=
|
ENSP00000270301.6:p.Gly1076=
|
|
ENST00000401500.7:c.3241G=
MANE Select
|
ENSP00000384792.1:p.Gly1081=
|
|
ENST00000587391.6:c.*3101G=
|
ENSP00000465525.1:n.*3101G=
|
|
ENST00000679357.1:c.1321G=
|
|
|
ENST00000679598.1:c.6G=
|
|
|
ENST00000679682.1:c.3226G=
|
ENSP00000506226.1:p.Gly1076=
|
|
ENST00000679714.1:c.3235G=
|
ENSP00000506627.1:p.Gly1079=
|
|
ENST00000679757.1:c.2890G=
|
ENSP00000505158.1:p.Gly964=
|
|
ENST00000679858.1:c.*2623G=
|
ENSP00000505655.1:n.*2623G=
|
|
ENST00000680211.1:c.-159G=
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ENSP00000506102.1:n.-159G=
|
|
ENST00000680280.1:n.528G=
|
|
|
ENST00000680349.1:n.1809G=
|
|
|
ENST00000680403.1:c.3226G=
|
ENSP00000505677.1:p.Gly1076=
|
|
ENST00000680564.1:c.2992G=
|
ENSP00000505582.1:p.Gly998=
|
|
ENST00000680590.1:c.*1621G=
|
ENSP00000505350.1:n.*1621G=
|
|
ENST00000680597.1:c.6G=
|
|
|
ENST00000680739.1:c.256G=
|
|
|
ENST00000680773.1:n.1742G=
|
|
|
ENST00000680806.1:c.*2544G=
|
ENSP00000506418.1:n.*2544G=
|
|
ENST00000680997.1:n.1173G=
|
|
|
ENST00000681608.1:n.774G=
|
|
|
ENST00000681625.1:c.*573G=
|
ENSP00000505555.1:n.*573G=
|
|
ENST00000681648.1:n.540G=
|
|
|
ENST00000270301.11:c.3226G=
|
ENSP00000270301.6:p.Gly1076=
|
|
ENST00000401500.6:c.3241G=
|
ENSP00000384792.1:p.Gly1081=
|
|
ENST00000587391.5:c.*3101G=
|
ENSP00000465525.1:n.*3101G=
|
|
NM_001083961.1:c.3241G=
|
NP_001077430.1:p.Gly1081=
|
|
NM_173636.4:c.3226G=
|
NP_775907.4:p.Gly1076=
|
|
XM_005258809.2:c.3130G=
|
XP_005258866.1:p.Gly1044=
|
|
XM_011526837.1:c.3226G=
|
XP_011525139.1:p.Gly1076=
|
|
XM_011526838.1:c.2992G=
|
XP_011525140.1:p.Gly998=
|
|
XM_011526839.1:c.2890G=
|
XP_011525141.1:p.Gly964=
|
|
XM_011526840.1:c.2233G=
|
XP_011525142.1:p.Gly745=
|
|
XM_011526841.1:c.1819G=
|
XP_011525143.1:p.Gly607=
|
|
XM_011526842.1:c.1672G=
|
XP_011525144.1:p.Gly558=
|
|
XM_011526843.1:c.988G=
|
XP_011525145.1:p.Gly330=
|
|
XM_011526844.1:c.988G=
|
XP_011525146.1:p.Gly330=
|
|
XM_011526840.2:c.2233G=
|
XP_011525142.1:p.Gly745=
|
|
XM_011526841.2:c.1819G=
|
XP_011525143.1:p.Gly607=
|
|
XM_011526844.2:c.988G=
|
XP_011525146.1:p.Gly330=
|
|
XM_017026665.1:c.3241G=
|
XP_016882154.1:p.Gly1081=
|
|
NM_001083961.2:c.3241G=
MANE Select
|
NP_001077430.1:p.Gly1081=
|
|
NM_173636.5:c.3226G=
|
NP_775907.4:p.Gly1076=
|
|