|
ENST00000478464.6:c.560G>T
|
ENSP00000419303.2:p.Gly187Val
|
|
|
ENST00000480644.2:c.686G>T
|
ENSP00000420229.2:p.Gly229Val
|
|
|
ENST00000492644.2:n.3024G>T
|
|
|
|
ENST00000684961.1:c.389G>T
|
ENSP00000508439.1:p.Gly130Val
|
|
|
ENST00000686433.1:c.716G>T
|
ENSP00000509173.1:p.Gly239Val
|
|
|
ENST00000687538.1:c.560G>T
|
ENSP00000508887.1:p.Gly187Val
|
|
|
ENST00000688697.1:c.770G>T
|
ENSP00000510396.1:p.Gly257Val
|
|
|
ENST00000689286.1:c.560G>T
|
ENSP00000509897.1:p.Gly187Val
|
|
|
ENST00000689925.1:c.*111G>T
|
ENSP00000510082.1:n.*111G>T
|
|
|
ENST00000690298.1:c.*411G>T
|
ENSP00000509376.1:n.*411G>T
|
|
|
ENST00000691070.1:c.686G>T
|
ENSP00000509723.1:p.Gly229Val
|
|
|
ENST00000692727.1:n.3292G>T
|
|
|
|
ENST00000693155.1:n.1447G>T
|
|
|
|
ENST00000310776.9:c.767G>T
|
ENSP00000310785.5:p.Gly256Val
|
|
|
ENST00000680020.1:c.770G>T
MANE Select
|
ENSP00000505414.1:p.Gly257Val
|
|
|
ENST00000310776.8:c.770G>T
|
ENSP00000310785.4:p.Gly257Val
|
|
|
ENST00000465056.5:c.767G>T
|
ENSP00000418233.1:p.Gly256Val
|
|
|
ENST00000478464.5:c.647G>T
|
ENSP00000419303.1:p.Gly216Val
|
|
|
ENST00000480644.1:c.255G>T
|
|
|
|
ENST00000480938.5:n.1424G>T
|
|
|
|
ENST00000492644.1:n.1815G>T
|
|
|
|
ENST00000495075.5:c.770G>T
|
ENSP00000418008.1:p.Gly257Val
|
|
|
ENST00000498505.5:c.*367G>T
|
ENSP00000420482.1:n.*367G>T
|
|
|
NM_020191.2:c.770G>T
|
NP_064576.1:p.Gly257Val
|
|
|
XM_005247640.2:c.767G>T
|
XP_005247697.1:p.Gly256Val
|
|
|
XM_006713703.2:c.716G>T
|
XP_006713766.1:p.Gly239Val
|
|
|
XM_011512995.1:c.647G>T
|
XP_011511297.1:p.Gly216Val
|
|
|
XM_011512996.1:c.644G>T
|
XP_011511298.1:p.Gly215Val
|
|
|
NM_001363857.1:c.647G>T
|
NP_001350786.1:p.Gly216Val
|
|
|
NM_001363893.1:c.767G>T
|
NP_001350822.1:p.Gly256Val
|
|
|
NM_020191.3:c.770G>T
|
NP_064576.1:p.Gly257Val
|
|
|
XM_006713703.4:c.716G>T
|
XP_006713766.1:p.Gly239Val
|
|
|
XM_011512996.2:c.644G>T
|
XP_011511298.1:p.Gly215Val
|
|
|
NM_020191.4:c.770G>T
MANE Select
|
NP_064576.1:p.Gly257Val
|
|
