|
ENST00000269571.10:c.3671A>G
MANE Select
|
ENSP00000269571.4:p.Asp1224Gly
|
|
|
ENST00000269571.9:c.3671A>G
|
ENSP00000269571.4:p.Asp1224Gly
|
|
|
ENST00000406381.6:c.3581A>G
|
ENSP00000385185.2:p.Asp1194Gly
|
|
|
ENST00000445658.6:c.2843A>G
|
ENSP00000404047.2:p.Asp948Gly
|
|
|
ENST00000541774.5:c.3626A>G
|
ENSP00000446466.1:p.Asp1209Gly
|
|
|
ENST00000578373.5:c.*3461A>G
|
ENSP00000463427.1:n.*3461A>G
|
|
|
ENST00000584450.5:c.*250A>G
|
ENSP00000463714.1:n.*250A>G
|
|
|
ENST00000584601.5:c.3581A>G
|
ENSP00000462438.1:p.Asp1194Gly
|
|
|
NM_001005862.2:c.3581A>G , LRG_724t1:c.3581A>G
|
NP_001005862.1:p.Asp1194Gly
|
|
|
NM_001289936.1:c.3626A>G , LRG_724t4:c.3626A>G
|
NP_001276865.1:p.Asp1209Gly
|
|
|
NM_001289937.1:c.*250A>G
|
NP_001276866.1:n.*250A>G
|
|
|
NM_004448.3:c.3671A>G , LRG_724t2:c.3671A>G
|
NP_004439.2:p.Asp1224Gly
|
|
|
NR_110535.1:n.3995A>G
|
|
|
|
XM_024450641.1:c.3809A>G
|
XP_024306409.1:p.Asp1270Gly
|
|
|
XM_024450642.1:c.3764A>G
|
XP_024306410.1:p.Asp1255Gly
|
|
|
XM_024450643.1:c.3719A>G
|
XP_024306411.1:p.Asp1240Gly
|
|
|
NM_001005862.3:c.3581A>G
|
NP_001005862.1:p.Asp1194Gly
|
|
|
NM_001289936.2:c.3626A>G
|
NP_001276865.1:p.Asp1209Gly
|
|
|
NM_001289937.2:c.*250A>G
|
NP_001276866.1:n.*250A>G
|
|
|
NM_001382782.1:c.3581A>G
|
NP_001369711.1:p.Asp1194Gly
|
|
|
NM_001382783.1:c.3581A>G
|
NP_001369712.1:p.Asp1194Gly
|
|
|
NM_001382784.1:c.3788A>G
|
NP_001369713.1:p.Asp1263Gly
|
|
|
NM_001382785.1:c.3773A>G
|
NP_001369714.1:p.Asp1258Gly
|
|
|
NM_001382786.1:c.3752A>G
|
NP_001369715.1:p.Asp1251Gly
|
|
|
NM_001382787.1:c.3746A>G
|
NP_001369716.1:p.Asp1249Gly
|
|
|
NM_001382788.1:c.3701A>G
|
NP_001369717.1:p.Asp1234Gly
|
|
|
NM_001382789.1:c.3692A>G
|
NP_001369718.1:p.Asp1231Gly
|
|
|
NM_001382790.1:c.3668A>G
|
NP_001369719.1:p.Asp1223Gly
|
|
|
NM_001382791.1:c.3662A>G
|
NP_001369720.1:p.Asp1221Gly
|
|
|
NM_001382792.1:c.3635A>G
|
NP_001369721.1:p.Asp1212Gly
|
|
|
NM_001382793.1:c.3629A>G
|
NP_001369722.1:p.Asp1210Gly
|
|
|
NM_001382794.1:c.3629A>G
|
NP_001369723.1:p.Asp1210Gly
|
|
|
NM_001382795.1:c.3623A>G
|
NP_001369724.1:p.Asp1208Gly
|
|
|
NM_001382796.1:c.3584A>G
|
NP_001369725.1:p.Asp1195Gly
|
|
|
NM_001382797.1:c.3572A>G
|
NP_001369726.1:p.Asp1191Gly
|
|
|
NM_001382798.1:c.3515A>G
|
NP_001369727.1:p.Asp1172Gly
|
|
|
NM_001382799.1:c.3491A>G
|
NP_001369728.1:p.Asp1164Gly
|
|
|
NM_001382800.1:c.3485A>G
|
NP_001369729.1:p.Asp1162Gly
|
|
|
NM_001382801.1:c.3467A>G
|
NP_001369730.1:p.Asp1156Gly
|
|
|
NM_001382802.1:c.3413A>G
|
NP_001369731.1:p.Asp1138Gly
|
|
|
NM_001382803.1:c.*250A>G
|
NP_001369732.1:n.*250A>G
|
|
|
NM_001382804.1:c.2843A>G
|
NP_001369733.1:p.Asp948Gly
|
|
|
NM_001382805.1:c.2720A>G
|
NP_001369734.1:p.Asp907Gly
|
|
|
NM_001382806.1:c.2633A>G
|
NP_001369735.1:p.Asp878Gly
|
|
|
NM_004448.4:c.3671A>G
MANE Select
|
NP_004439.2:p.Asp1224Gly
|
|
|
NR_110535.2:n.3909A>G
|
|
|
