ENST00000298910.12:c.6509G>T
MANE Select
|
ENSP00000298910.7:p.Gly2170Val
|
|
ENST00000636518.1:c.306G>T
|
|
|
ENST00000679360.1:c.*5418G>T
|
ENSP00000505368.1:n.*5418G>T
|
|
ENST00000679532.1:c.2283G>T
|
|
|
ENST00000679683.1:c.299G>T
|
|
|
ENST00000680018.1:c.1954G>T
|
ENSP00000505347.1:n.1954G>T
|
|
ENST00000680422.1:c.2154G>T
|
|
|
ENST00000680425.1:c.1676G>T
|
ENSP00000506459.1:n.1676G>T
|
|
ENST00000680453.1:c.1966G>T
|
|
|
ENST00000680790.1:c.6254G>T
|
ENSP00000505335.1:p.Gly2085Val
|
|
ENST00000681136.1:n.2493G>T
|
|
|
ENST00000681696.1:c.2192G>T
|
ENSP00000505871.1:p.Gly731Val
|
|
ENST00000298910.11:c.6509G>T
|
ENSP00000298910.7:p.Gly2170Val
|
|
ENST00000430804.5:c.3805G>T
|
|
|
ENST00000479187.5:n.3190G>T
|
|
|
NM_198578.3:c.6509G>T
|
NP_940980.3:p.Gly2170Val
|
|
XM_005268629.2:c.6509G>T
|
XP_005268686.1:p.Gly2170Val
|
|
XM_011537877.1:c.6509G>T
|
XP_011536179.1:p.Gly2170Val
|
|
XM_011537878.1:c.6509G>T
|
XP_011536180.1:p.Gly2170Val
|
|
XM_011537879.1:c.5306G>T
|
XP_011536181.1:p.Gly1769Val
|
|
XM_005268629.4:c.6509G>T
|
XP_005268686.1:p.Gly2170Val
|
|
XM_011537877.3:c.6509G>T
|
XP_011536179.1:p.Gly2170Val
|
|
XM_017018787.1:c.3425G>T
|
XP_016874276.1:p.Gly1142Val
|
|
XM_017018788.2:c.2771G>T
|
XP_016874277.1:p.Gly924Val
|
|
XM_024448833.1:c.5306G>T
|
XP_024304601.1:p.Gly1769Val
|
|
NM_198578.4:c.6509G>T
MANE Select
|
NP_940980.4:p.Gly2170Val
|
|