|
ENST00000222399.11:c.1547G>C
MANE Select
|
ENSP00000222399.6:p.Gly516Ala
|
|
|
ENST00000393561.6:c.1136G>C
|
ENSP00000377191.2:p.Gly379Ala
|
|
|
ENST00000439976.6:c.1805G>C
|
ENSP00000412686.2:p.Gly602Ala
|
|
|
ENST00000676574.1:c.1547G>C
|
ENSP00000503081.1:p.Gly516Ala
|
|
|
ENST00000676777.1:c.1547G>C
|
ENSP00000504756.1:p.Gly516Ala
|
|
|
ENST00000676920.1:c.1136G>C
|
ENSP00000503814.1:p.Gly379Ala
|
|
|
ENST00000677101.1:c.*1183G>C
|
ENSP00000503156.1:n.*1183G>C
|
|
|
ENST00000677144.1:c.1547G>C
|
ENSP00000503049.1:p.Gly516Ala
|
|
|
ENST00000677485.1:n.2771G>C
|
|
|
|
ENST00000677588.1:c.1547G>C
|
ENSP00000502938.1:p.Gly516Ala
|
|
|
ENST00000677652.1:n.1736G>C
|
|
|
|
ENST00000677734.1:n.1736G>C
|
|
|
|
ENST00000677793.1:c.1547G>C
|
ENSP00000504020.1:p.Gly516Ala
|
|
|
ENST00000677801.1:c.1136G>C
|
ENSP00000503438.1:p.Gly379Ala
|
|
|
ENST00000677994.1:n.1713G>C
|
|
|
|
ENST00000678232.1:n.1736G>C
|
|
|
|
ENST00000678266.1:n.1689G>C
|
|
|
|
ENST00000678346.1:c.*1183G>C
|
ENSP00000504349.1:n.*1183G>C
|
|
|
ENST00000678698.1:c.1136G>C
|
ENSP00000503198.1:p.Gly379Ala
|
|
|
ENST00000678704.1:c.*129G>C
|
ENSP00000504589.1:n.*129G>C
|
|
|
ENST00000678892.1:c.1547G>C
|
ENSP00000504841.1:p.Gly516Ala
|
|
|
ENST00000679173.1:n.1736G>C
|
|
|
|
ENST00000679200.1:c.1136G>C
|
ENSP00000503498.1:p.Gly379Ala
|
|
|
ENST00000679244.1:c.1547G>C
|
ENSP00000504656.1:p.Gly516Ala
|
|
|
ENST00000222399.10:c.1547G>C
|
ENSP00000222399.6:p.Gly516Ala
|
|
|
ENST00000393560.5:c.1547G>C
|
ENSP00000377190.1:p.Gly516Ala
|
|
|
ENST00000393561.5:c.1619G>C
|
ENSP00000377191.1:p.Gly540Ala
|
|
|
NM_002291.2:c.1547G>C
|
NP_002282.2:p.Gly516Ala
|
|
|
XM_011516203.1:c.1547G>C
|
XP_011514505.1:p.Gly516Ala
|
|
|
XM_017012201.1:c.1619G>C
|
XP_016867690.1:p.Gly540Ala
|
|
|
XM_017012202.1:c.1619G>C
|
XP_016867691.1:p.Gly540Ala
|
|
|
XR_001744756.1:n.2350G>C
|
|
|
|
NM_002291.3:c.1547G>C
MANE Select
|
NP_002282.2:p.Gly516Ala
|
|
