ENST00000327892.13:c.773T>G
MANE Select
|
ENSP00000339001.7:p.Val258Gly
|
|
ENST00000680530.1:n.1635T>G
|
|
|
ENST00000681421.1:n.1839T>G
|
|
|
ENST00000681435.1:c.557T>G
|
ENSP00000506665.1:p.Val186Gly
|
|
ENST00000327892.12:c.773T>G
|
ENSP00000339001.7:p.Val258Gly
|
|
ENST00000330914.7:c.557T>G
|
ENSP00000365578.2:p.Val186Gly
|
|
ENST00000396384.1:c.557T>G
|
ENSP00000379668.1:p.Val186Gly
|
|
ENST00000396389.5:c.719T>G
|
ENSP00000379672.1:p.Val240Gly
|
|
NM_001293212.1:c.833T>G
|
NP_001280141.1:p.Val278Gly
|
|
NM_001293213.1:c.370-203T>G
|
NP_001280142.1:n.370-203T>G
|
|
NM_001293214.1:c.641T>G
|
NP_001280143.1:p.Val214Gly
|
|
NM_001293215.1:c.557T>G
|
NP_001280144.1:p.Val186Gly
|
|
NM_001293216.1:c.557T>G
|
NP_001280145.1:p.Val186Gly
|
|
NM_178014.3:c.773T>G
|
NP_821133.1:p.Val258Gly
|
|
NR_120608.1:n.584-104T>G
|
|
|
NM_178014.4:c.773T>G
MANE Select
|
NP_821133.1:p.Val258Gly
|
|
NM_001293212.2:c.833T>G
|
NP_001280141.1:p.Val278Gly
|
|
NM_001293213.2:c.370-203T>G
|
NP_001280142.1:n.370-203T>G
|
|
NM_001293214.2:c.641T>G
|
NP_001280143.1:p.Val214Gly
|
|
NM_001293215.2:c.557T>G
|
NP_001280144.1:p.Val186Gly
|
|
NM_001293216.2:c.557T>G
|
NP_001280145.1:p.Val186Gly
|
|
NR_120608.2:n.433-104T>G
|
|
|