|
ENST00000703936.1:c.2647C>G
|
ENSP00000515567.1:p.Arg883Gly
|
|
|
ENST00000703937.1:c.*1708C>G
|
ENSP00000515568.1:n.*1708C>G
|
|
|
ENST00000326739.9:c.607C>G
MANE Select
|
ENSP00000321584.4:p.Arg203Gly
|
|
|
ENST00000429182.6:c.607C>G
|
ENSP00000393525.2:p.Arg203Gly
|
|
|
ENST00000442157.2:c.532C>G
|
ENSP00000403502.2:p.Arg178Gly
|
|
|
ENST00000462980.2:n.1122C>G
|
|
|
|
ENST00000472328.2:n.673C>G
|
|
|
|
ENST00000491610.2:n.494C>G
|
|
|
|
ENST00000676607.1:n.903C>G
|
|
|
|
ENST00000676627.1:n.1337C>G
|
|
|
|
ENST00000676708.1:n.1814C>G
|
|
|
|
ENST00000676864.1:n.1683C>G
|
|
|
|
ENST00000677010.1:c.643C>G
|
ENSP00000503089.1:p.Arg215Gly
|
|
|
ENST00000677108.1:n.2440C>G
|
|
|
|
ENST00000677168.1:n.1079C>G
|
|
|
|
ENST00000677185.1:n.1097C>G
|
|
|
|
ENST00000677205.1:n.1318C>G
|
|
|
|
ENST00000677344.1:n.1808C>G
|
|
|
|
ENST00000677480.1:c.*284C>G
|
ENSP00000504378.1:n.*284C>G
|
|
|
ENST00000677519.1:n.1317C>G
|
|
|
|
ENST00000677593.1:n.1090C>G
|
|
|
|
ENST00000677740.1:n.2039C>G
|
|
|
|
ENST00000677991.1:n.1780C>G
|
|
|
|
ENST00000678001.1:n.1100C>G
|
|
|
|
ENST00000678085.1:n.1090C>G
|
|
|
|
ENST00000678177.1:n.2383C>G
|
|
|
|
ENST00000678603.1:n.1685C>G
|
|
|
|
ENST00000678724.1:c.532C>G
|
ENSP00000503874.1:p.Arg178Gly
|
|
|
ENST00000678920.1:n.765C>G
|
|
|
|
ENST00000679019.1:n.1304C>G
|
|
|
|
ENST00000679117.1:c.*422C>G
|
ENSP00000503240.1:n.*422C>G
|
|
|
ENST00000679339.1:n.1375C>G
|
|
|
|
ENST00000326739.8:c.607C>G
|
ENSP00000321584.4:p.Arg203Gly
|
|
|
ENST00000429182.5:c.401C>G
|
|
|
|
ENST00000442157.1:c.532C>G
|
ENSP00000403502.1:p.Arg178Gly
|
|
|
ENST00000462980.1:n.509C>G
|
|
|
|
ENST00000491610.1:n.494C>G
|
|
|
|
NM_000884.2:c.607C>G
|
NP_000875.2:p.Arg203Gly
|
|
|
XM_006713128.2:c.817C>G
|
XP_006713191.1:p.Arg273Gly
|
|
|
XM_006713128.3:c.817C>G
|
XP_006713191.1:p.Arg273Gly
|
|
|
XM_017006349.1:c.742C>G
|
XP_016861838.1:p.Arg248Gly
|
|
|
XM_017006350.1:c.742C>G
|
XP_016861839.1:p.Arg248Gly
|
|
|
NM_000884.3:c.607C>G
MANE Select
|
NP_000875.2:p.Arg203Gly
|
|
