ENST00000298910.12:c.4974T>G
MANE Select
|
ENSP00000298910.7:p.Ile1658Met
|
|
ENST00000679360.1:c.*3883T>G
|
ENSP00000505368.1:n.*3883T>G
|
|
ENST00000679532.1:c.748T>G
|
|
|
ENST00000680018.1:c.419T>G
|
ENSP00000505347.1:n.419T>G
|
|
ENST00000680422.1:c.619T>G
|
|
|
ENST00000680425.1:c.183-900T>G
|
ENSP00000506459.1:n.183-900T>G
|
|
ENST00000680453.1:c.473-900T>G
|
|
|
ENST00000680790.1:c.4719T>G
|
ENSP00000505335.1:p.Ile1573Met
|
|
ENST00000681136.1:n.958T>G
|
|
|
ENST00000681696.1:c.657T>G
|
ENSP00000505871.1:p.Ile219Met
|
|
ENST00000298910.11:c.4974T>G
|
ENSP00000298910.7:p.Ile1658Met
|
|
ENST00000430804.5:c.2270T>G
|
|
|
ENST00000479187.5:n.1655T>G
|
|
|
NM_198578.3:c.4974T>G
|
NP_940980.3:p.Ile1658Met
|
|
XM_005268629.2:c.4974T>G
|
XP_005268686.1:p.Ile1658Met
|
|
XM_011537877.1:c.4974T>G
|
XP_011536179.1:p.Ile1658Met
|
|
XM_011537878.1:c.4974T>G
|
XP_011536180.1:p.Ile1658Met
|
|
XM_011537879.1:c.3771T>G
|
XP_011536181.1:p.Ile1257Met
|
|
XM_011537881.1:c.4828-900T>G
|
XP_011536183.1:n.4828-900T>G
|
|
XM_005268629.4:c.4974T>G
|
XP_005268686.1:p.Ile1658Met
|
|
XM_011537877.3:c.4974T>G
|
XP_011536179.1:p.Ile1658Met
|
|
XM_011537881.3:c.4828-900T>G
|
XP_011536183.1:n.4828-900T>G
|
|
XM_017018787.1:c.1890T>G
|
XP_016874276.1:p.Ile630Met
|
|
XM_017018788.2:c.1236T>G
|
XP_016874277.1:p.Ile412Met
|
|
XM_024448833.1:c.3771T>G
|
XP_024304601.1:p.Ile1257Met
|
|
XR_001748574.2:n.5342T>G
|
|
|
NM_198578.4:c.4974T>G
MANE Select
|
NP_940980.4:p.Ile1658Met
|
|