ENST00000682266.1:c.1361G>T
|
ENSP00000507766.1:p.Gly454Val
|
|
ENST00000682341.1:c.1769G>T
|
ENSP00000508251.1:p.Gly590Val
|
|
ENST00000683197.1:c.1769G>T
|
ENSP00000507641.1:p.Gly590Val
|
|
ENST00000683411.1:c.1361G>T
|
ENSP00000508397.1:p.Gly454Val
|
|
ENST00000683437.1:c.1361G>T
|
ENSP00000508408.1:p.Gly454Val
|
|
ENST00000683613.1:n.2805G>T
|
|
|
ENST00000684663.1:c.1766G>T
|
ENSP00000508009.1:p.Gly589Val
|
|
ENST00000324559.9:c.1811G>T
MANE Select
|
ENSP00000315371.9:p.Gly604Val
|
|
ENST00000648804.1:n.2146G>T
|
|
|
ENST00000324559.8:c.1811G>T
|
ENSP00000315371.8:p.Gly604Val
|
|
NM_001142649.1:c.1808G>T
|
NP_001136121.1:p.Gly603Val
|
|
NM_213599.2:c.1811G>T , LRG_868t1:c.1811G>T
|
NP_998764.1:p.Gly604Val
|
|
XM_005252820.2:c.1769G>T
|
XP_005252877.2:p.Gly590Val
|
|
XM_005252821.2:c.1766G>T
|
XP_005252878.2:p.Gly589Val
|
|
XM_005252822.3:c.1733G>T
|
XP_005252879.1:p.Gly578Val
|
|
XM_005252823.3:c.1730G>T
|
XP_005252880.1:p.Gly577Val
|
|
XM_011519949.1:c.1718G>T
|
XP_011518251.1:p.Gly573Val
|
|
XM_005252820.3:c.1769G>T
|
XP_005252877.2:p.Gly590Val
|
|
XM_005252821.3:c.1766G>T
|
XP_005252878.2:p.Gly589Val
|
|
XM_005252822.4:c.1733G>T
|
XP_005252879.1:p.Gly578Val
|
|
XM_011519949.2:c.1718G>T
|
XP_011518251.1:p.Gly573Val
|
|
NM_001142649.2:c.1808G>T
|
NP_001136121.1:p.Gly603Val
|
|
NM_213599.3:c.1811G>T
MANE Select
|
NP_998764.1:p.Gly604Val
|
|