ENST00000426508.7:c.3827G>T
MANE Select
|
ENSP00000406012.2:p.Gly1276Val
|
|
ENST00000361339.9:c.1409G>T
|
ENSP00000354895.5:p.Gly470Val
|
|
ENST00000397417.6:c.*2265G>T
|
ENSP00000380562.2:n.*2265G>T
|
|
ENST00000426508.6:c.3827G>T
|
ENSP00000406012.2:p.Gly1276Val
|
|
ENST00000565298.5:n.3651G>T
|
|
|
NM_014714.3:c.3827G>T
|
NP_055529.2:p.Gly1276Val
|
|
XM_006720989.2:c.3827G>T
|
XP_006721052.1:p.Gly1276Val
|
|
XM_006720990.2:c.3827G>T
|
XP_006721053.1:p.Gly1276Val
|
|
XM_006720991.2:c.3827G>T
|
XP_006721054.1:p.Gly1276Val
|
|
XM_006720992.2:c.1460G>T
|
XP_006721055.1:p.Gly487Val
|
|
XM_011522766.1:c.3581G>T
|
XP_011521068.1:p.Gly1194Val
|
|
XM_011522767.1:c.2852G>T
|
XP_011521069.1:p.Gly951Val
|
|
XM_006720990.3:c.3827G>T
|
XP_006721053.1:p.Gly1276Val
|
|
XM_006720991.3:c.3827G>T
|
XP_006721054.1:p.Gly1276Val
|
|
XM_006720992.3:c.1460G>T
|
XP_006721055.1:p.Gly487Val
|
|
XM_011522766.3:c.3581G>T
|
XP_011521068.1:p.Gly1194Val
|
|
XM_011522767.2:c.2852G>T
|
XP_011521069.1:p.Gly951Val
|
|
XM_017023910.1:c.3827G>T
|
XP_016879399.1:p.Gly1276Val
|
|
XM_017023911.1:c.2012G>T
|
XP_016879400.1:p.Gly671Val
|
|
NM_014714.4:c.3827G>T
MANE Select
|
NP_055529.2:p.Gly1276Val
|
|