ENST00000680821.2:c.3887G>T
MANE Select
|
ENSP00000504874.1:p.Gly1296Val
|
|
ENST00000262765.10:c.3389G>T
|
ENSP00000262765.5:p.Gly1130Val
|
|
ENST00000636395.1:c.3887G>T
|
ENSP00000490761.1:p.Gly1296Val
|
|
ENST00000680821.1:c.3887G>T
|
ENSP00000504874.1:p.Gly1296Val
|
|
ENST00000262765.9:c.3389G>T
|
ENSP00000262765.5:p.Gly1130Val
|
|
ENST00000447564.2:c.413G>T
|
ENSP00000394461.2:p.Gly138Val
|
|
ENST00000524722.1:c.*153G>T
|
ENSP00000432679.1:n.*153G>T
|
|
NM_032134.2:c.3389G>T
|
NP_115510.1:p.Gly1130Val
|
|
NR_130649.1:n.660G>T
|
|
|
XM_005257728.2:c.3887G>T
|
XP_005257785.1:p.Gly1296Val
|
|
XM_006722136.2:c.149G>T
|
XP_006722199.1:p.Gly50Val
|
|
XM_011525344.1:c.3167G>T
|
XP_011523646.1:p.Gly1056Val
|
|
XM_005257728.4:c.3887G>T
|
XP_005257785.1:p.Gly1296Val
|
|
XM_006722136.3:c.149G>T
|
XP_006722199.1:p.Gly50Val
|
|
XM_011525344.2:c.3167G>T
|
XP_011523646.1:p.Gly1056Val
|
|
XM_017025206.2:c.3887G>T
|
XP_016880695.1:p.Gly1296Val
|
|
XM_017025207.2:c.3827G>T
|
XP_016880696.1:p.Gly1276Val
|
|
XM_017025208.1:c.-80G>T
|
XP_016880697.1:n.-80G>T
|
|
NM_001388453.1:c.3887G>T
MANE Select
|
NP_001375382.1:p.Gly1296Val
|
|
NM_032134.3:c.3887G>T
|
NP_115510.2:p.Gly1296Val
|
|
NR_130649.2:n.1256G>T
|
|
|