ENST00000490131.7:c.2534A>G
|
ENSP00000418685.2:p.Asp845Gly
|
|
ENST00000498619.4:c.2795A>G
|
ENSP00000420194.1:p.Asp932Gly
|
|
ENST00000638421.1:c.2765A>G
|
ENSP00000492190.1:p.Asp922Gly
|
|
ENST00000639785.2:c.2765A>G
MANE Select
|
ENSP00000491584.2:p.Asp922Gly
|
|
ENST00000490131.5:c.2765A>G
|
ENSP00000418685.1:p.Asp922Gly
|
|
ENST00000498619.2:c.2795A>G
|
ENSP00000420194.1:p.Asp932Gly
|
|
NM_000388.3:c.2765A>G
|
NP_000379.2:p.Asp922Gly
|
|
NM_001178065.1:c.2795A>G
|
NP_001171536.1:p.Asp932Gly
|
|
XM_005247836.2:c.2765A>G
|
XP_005247893.1:p.Asp922Gly
|
|
XM_005247837.2:c.2282A>G
|
XP_005247894.1:p.Asp761Gly
|
|
XM_006713789.2:c.2765A>G
|
XP_006713852.1:p.Asp922Gly
|
|
XM_011513237.1:c.2765A>G
|
XP_011511539.1:p.Asp922Gly
|
|
XM_011513238.1:c.2765A>G
|
XP_011511540.1:p.Asp922Gly
|
|
XM_011513239.1:c.2177A>G
|
XP_011511541.1:p.Asp726Gly
|
|
XM_006713789.3:c.2765A>G
|
XP_006713852.1:p.Asp922Gly
|
|
XM_017007324.1:c.2765A>G
|
XP_016862813.1:p.Asp922Gly
|
|
XM_017007325.1:c.2765A>G
|
XP_016862814.1:p.Asp922Gly
|
|
NM_000388.4:c.2765A>G
MANE Select
|
NP_000379.3:p.Asp922Gly
|
|
NM_001178065.2:c.2795A>G
|
NP_001171536.2:p.Asp932Gly
|
|