|
NM_024537.4:c.781G>T
MANE Select
|
NP_078813.1:p.Ala261Ser
|
|
ENST00000257347.9:c.781G>T
MANE Select
|
ENSP00000257347.4:p.Ala261Ser
|
|
NM_001352252.1:c.-6G>T
|
NP_001339181.1:n.-6G>T
|
|
NM_001352252.2:c.-6G>T
|
NP_001339181.1:n.-6G>T
|
|
NM_001352253.1:c.781G>T
|
NP_001339182.1:p.Ala261Ser
|
|
NM_001352253.2:c.781G>T
|
NP_001339182.1:p.Ala261Ser
|
|
NM_001352253.3:c.781G>T
|
NP_001339182.1:p.Ala261Ser
|
|
NM_024537.2:c.781G>T
|
NP_078813.1:p.Ala261Ser
|
|
NM_024537.3:c.781G>T
|
NP_078813.1:p.Ala261Ser
|
|
NR_147941.1:n.752G>T
|
|
|
NR_147942.1:n.868G>T
|
|
|
NR_147942.2:n.804G>T
|
|
|
ENST00000257347.8:c.781G>T
|
ENSP00000257347.4:p.Ala261Ser
|
|
ENST00000465145.5:n.706G>T
|
|
|
ENST00000481787.6:n.215G>T
|
|
|
ENST00000535398.5:n.973G>T
|
|
|
ENST00000537743.1:c.47G>T
|
|
|
ENST00000539269.5:c.791G>T
|
|
|
ENST00000543487.5:n.297G>T
|
|
|
XM_006719953.2:c.442G>T
|
XP_006720016.1:p.Ala148Ser
|
|
XM_006719953.3:c.442G>T
|
XP_006720016.1:p.Ala148Ser
|
|
XM_011521114.1:c.781G>T
|
XP_011519416.1:p.Ala261Ser
|
|
XM_011521115.1:c.442G>T
|
XP_011519417.1:p.Ala148Ser
|
|
XM_011521116.1:c.436G>T
|
XP_011519418.1:p.Ala146Ser
|
|
XM_011521117.1:c.781G>T
|
XP_011519419.1:p.Ala261Ser
|
|
XM_011521117.3:c.781G>T
|
XP_011519419.1:p.Ala261Ser
|
|
XM_011521118.1:c.781G>T
|
XP_011519420.1:p.Ala261Ser
|
|
XM_011521118.3:c.781G>T
|
XP_011519420.1:p.Ala261Ser
|
|
XM_011521119.1:c.781G>T
|
XP_011519421.1:p.Ala261Ser
|
|
XM_011521120.1:c.-6G>T
|
XP_011519422.1:n.-6G>T
|
|
XM_017020741.1:c.442G>T
|
XP_016876230.1:p.Ala148Ser
|
|
XM_017020742.2:c.781G>T
|
XP_016876231.1:p.Ala261Ser
|
|
XM_024449409.1:c.-6G>T
|
XP_024305177.1:n.-6G>T
|
|
XR_001749664.2:n.821G>T
|
|
|
XR_001749665.2:n.821G>T
|
|
|
XR_001749666.2:n.821G>T
|
|
|
XR_001749667.2:n.821G>T
|
|
|
XR_001749668.2:n.821G>T
|
|
|
XR_002957472.1:n.821G>T
|
|
|
XR_243047.2:n.804G>T
|
|
|
XR_243047.3:n.821G>T
|
|
|
XR_243048.3:n.804G>T
|
|
|
XR_243048.4:n.821G>T
|
|
|
XR_243049.3:n.804G>T
|
|
|
XR_243049.4:n.821G>T
|
|
|
XR_243051.2:n.804G>T
|
|
|
XR_243051.3:n.821G>T
|
|
