ENST00000315212.4:c.538C>T
MANE Select
|
ENSP00000313350.3:p.Gln180Ter
|
|
ENST00000654051.1:c.538C>T
|
ENSP00000499604.1:p.Gln180Ter
|
|
ENST00000658393.1:c.538C>T
|
ENSP00000499330.1:p.Gln180Ter
|
|
ENST00000315212.3:c.538C>T
|
ENSP00000313350.3:p.Gln180Ter
|
|
ENST00000436842.5:c.*644C>T
|
ENSP00000404926.1:n.*644C>T
|
|
NM_001286834.1:c.460C>T
|
NP_001273763.1:p.Gln154Ter
|
|
NM_001286837.1:c.187C>T
|
NP_001273766.1:p.Gln63Ter
|
|
NM_002936.4:c.538C>T
|
NP_002927.2:p.Gln180Ter
|
|
XR_244873.1:n.645C>T
|
|
|
XR_922665.1:n.645C>T
|
|
|
XR_922666.1:n.645C>T
|
|
|
XR_922667.1:n.645C>T
|
|
|
XR_922668.1:n.645C>T
|
|
|
XR_922669.1:n.645C>T
|
|
|
XR_922670.1:n.645C>T
|
|
|
XR_922671.1:n.645C>T
|
|
|
XR_922672.1:n.645C>T
|
|
|
XR_922673.1:n.645C>T
|
|
|
XR_922674.1:n.645C>T
|
|
|
NM_001286834.2:c.460C>T
|
NP_001273763.1:p.Gln154Ter
|
|
NM_001286837.2:c.187C>T
|
NP_001273766.1:p.Gln63Ter
|
|
NM_002936.5:c.538C>T
|
NP_002927.2:p.Gln180Ter
|
|
NR_148532.1:n.649C>T
|
|
|
NR_148533.1:n.649C>T
|
|
|
NR_148534.1:n.649C>T
|
|
|
NM_001286837.3:c.187C>T
|
NP_001273766.1:p.Gln63Ter
|
|
NR_148532.2:n.611C>T
|
|
|
NR_148533.2:n.611C>T
|
|
|
NR_148534.2:n.611C>T
|
|
|
NM_001286834.3:c.460C>T
|
NP_001273763.1:p.Gln154Ter
|
|
NM_001378271.1:c.538C>T
|
NP_001365200.1:p.Gln180Ter
|
|
NM_001378272.1:c.535C>T
|
NP_001365201.1:p.Gln179Ter
|
|
NM_001378273.1:c.523C>T
|
NP_001365202.1:p.Gln175Ter
|
|
NM_002936.6:c.538C>T
MANE Select
|
NP_002927.2:p.Gln180Ter
|
|
NR_165465.1:n.495C>T
|
|
|
NR_165466.1:n.583-3C>T
|
|
|
NR_165467.1:n.780C>T
|
|
|
NR_165468.1:n.583C>T
|
|
|