ENST00000298910.12:c.4996T>G
MANE Select
|
ENSP00000298910.7:p.Tyr1666Asp
|
|
ENST00000679360.1:c.*3905T>G
|
ENSP00000505368.1:n.*3905T>G
|
|
ENST00000679532.1:c.770T>G
|
|
|
ENST00000680018.1:c.441T>G
|
ENSP00000505347.1:n.441T>G
|
|
ENST00000680422.1:c.641T>G
|
|
|
ENST00000680425.1:c.183-878T>G
|
ENSP00000506459.1:n.183-878T>G
|
|
ENST00000680453.1:c.473-878T>G
|
|
|
ENST00000680790.1:c.4741T>G
|
ENSP00000505335.1:p.Tyr1581Asp
|
|
ENST00000681136.1:n.980T>G
|
|
|
ENST00000681696.1:c.679T>G
|
ENSP00000505871.1:p.Tyr227Asp
|
|
ENST00000298910.11:c.4996T>G
|
ENSP00000298910.7:p.Tyr1666Asp
|
|
ENST00000430804.5:c.2292T>G
|
|
|
ENST00000479187.5:n.1677T>G
|
|
|
NM_198578.3:c.4996T>G
|
NP_940980.3:p.Tyr1666Asp
|
|
XM_005268629.2:c.4996T>G
|
XP_005268686.1:p.Tyr1666Asp
|
|
XM_011537877.1:c.4996T>G
|
XP_011536179.1:p.Tyr1666Asp
|
|
XM_011537878.1:c.4996T>G
|
XP_011536180.1:p.Tyr1666Asp
|
|
XM_011537879.1:c.3793T>G
|
XP_011536181.1:p.Tyr1265Asp
|
|
XM_011537881.1:c.4828-878T>G
|
XP_011536183.1:n.4828-878T>G
|
|
XM_005268629.4:c.4996T>G
|
XP_005268686.1:p.Tyr1666Asp
|
|
XM_011537877.3:c.4996T>G
|
XP_011536179.1:p.Tyr1666Asp
|
|
XM_011537881.3:c.4828-878T>G
|
XP_011536183.1:n.4828-878T>G
|
|
XM_017018787.1:c.1912T>G
|
XP_016874276.1:p.Tyr638Asp
|
|
XM_017018788.2:c.1258T>G
|
XP_016874277.1:p.Tyr420Asp
|
|
XM_024448833.1:c.3793T>G
|
XP_024304601.1:p.Tyr1265Asp
|
|
XR_001748574.2:n.5364T>G
|
|
|
NM_198578.4:c.4996T>G
MANE Select
|
NP_940980.4:p.Tyr1666Asp
|
|