|
NM_024537.4:c.1061A>G
MANE Select
|
NP_078813.1:p.Asp354Gly
|
|
ENST00000257347.9:c.1061A>G
MANE Select
|
ENSP00000257347.4:p.Asp354Gly
|
|
NM_001352252.1:c.275A>G
|
NP_001339181.1:p.Asp92Gly
|
|
NM_001352252.2:c.275A>G
|
NP_001339181.1:p.Asp92Gly
|
|
NM_024537.2:c.1061A>G
|
NP_078813.1:p.Asp354Gly
|
|
NM_024537.3:c.1061A>G
|
NP_078813.1:p.Asp354Gly
|
|
NR_147941.1:n.1032A>G
|
|
|
NR_147942.1:n.1306A>G
|
|
|
NR_147942.2:n.1242A>G
|
|
|
ENST00000257347.8:c.1061A>G
|
ENSP00000257347.4:p.Asp354Gly
|
|
ENST00000375781.9:n.332A>G
|
|
|
ENST00000481787.6:n.495A>G
|
|
|
ENST00000487253.6:c.142A>G
|
|
|
ENST00000535398.5:n.1253A>G
|
|
|
ENST00000535516.5:n.551A>G
|
|
|
ENST00000535615.5:n.345A>G
|
|
|
ENST00000537386.1:n.185A>G
|
|
|
ENST00000537404.1:n.181A>G
|
|
|
ENST00000537802.5:n.1345A>G
|
|
|
ENST00000540006.5:n.485A>G
|
|
|
ENST00000541362.5:n.285A>G
|
|
|
ENST00000543487.5:n.577A>G
|
|
|
ENST00000545506.5:n.406A>G
|
|
|
XM_006719953.2:c.722A>G
|
XP_006720016.1:p.Asp241Gly
|
|
XM_006719953.3:c.722A>G
|
XP_006720016.1:p.Asp241Gly
|
|
XM_011521114.1:c.1061A>G
|
XP_011519416.1:p.Asp354Gly
|
|
XM_011521115.1:c.722A>G
|
XP_011519417.1:p.Asp241Gly
|
|
XM_011521116.1:c.716A>G
|
XP_011519418.1:p.Asp239Gly
|
|
XM_011521120.1:c.275A>G
|
XP_011519422.1:p.Asp92Gly
|
|
XM_017020741.1:c.722A>G
|
XP_016876230.1:p.Asp241Gly
|
|
XM_017020742.2:c.994A>G
|
XP_016876231.1:p.Thr332Ala
|
|
XM_024449409.1:c.275A>G
|
XP_024305177.1:p.Asp92Gly
|
|
XR_001749664.2:n.1101A>G
|
|
|
XR_001749665.2:n.1101A>G
|
|
|
XR_001749666.2:n.1101A>G
|
|
|
XR_001749667.2:n.1101A>G
|
|
|
XR_001749668.2:n.1034A>G
|
|
|
XR_002957472.1:n.1034A>G
|
|
|
XR_243047.2:n.1084A>G
|
|
|
XR_243047.3:n.1101A>G
|
|
|
XR_243048.3:n.1084A>G
|
|
|
XR_243048.4:n.1101A>G
|
|
|
XR_243049.3:n.1084A>G
|
|
|
XR_243049.4:n.1101A>G
|
|
|
XR_243051.2:n.1017A>G
|
|
|
XR_243051.3:n.1034A>G
|
|
