ENST00000646893.2:c.985G>T
|
ENSP00000494249.2:p.Ala329Ser
|
|
ENST00000428343.6:c.646G>T
MANE Select
|
ENSP00000401536.1:p.Ala216Ser
|
|
ENST00000646446.1:c.859G>T
|
ENSP00000494216.1:p.Ala287Ser
|
|
ENST00000646893.1:c.772G>T
|
ENSP00000494249.1:p.Ala258Ser
|
|
ENST00000428343.5:c.646G>T
|
ENSP00000401536.1:p.Ala216Ser
|
|
ENST00000481179.5:c.*362G>T
|
ENSP00000422968.1:n.*362G>T
|
|
NM_001145664.1:c.646G>T
|
NP_001139136.1:p.Ala216Ser
|
|
XM_011511771.1:c.874G>T
|
XP_011510073.1:p.Ala292Ser
|
|
XM_011511772.1:c.859G>T
|
XP_011510074.1:p.Ala287Ser
|
|
XM_011511773.1:c.556G>T
|
XP_011510075.1:p.Ala186Ser
|
|
XM_011511774.1:c.874G>T
|
XP_011510076.1:p.Ala292Ser
|
|
XM_011511775.1:c.874G>T
|
XP_011510077.1:p.Ala292Ser
|
|
XM_011511776.1:c.358G>T
|
XP_011510078.1:p.Ala120Ser
|
|
XM_011511777.1:c.358G>T
|
XP_011510079.1:p.Ala120Ser
|
|
XM_011511778.1:c.358G>T
|
XP_011510080.1:p.Ala120Ser
|
|
XM_011511779.1:c.*59G>T
|
XP_011510081.1:n.*59G>T
|
|
XM_011511771.2:c.874G>T
|
XP_011510073.1:p.Ala292Ser
|
|
XM_011511777.2:c.358G>T
|
XP_011510079.1:p.Ala120Ser
|
|
XM_017004851.1:c.985G>T
|
XP_016860340.1:p.Ala329Ser
|
|
XM_017004852.1:c.772G>T
|
XP_016860341.1:p.Ala258Ser
|
|
XM_017004853.1:c.985G>T
|
XP_016860342.1:p.Ala329Ser
|
|
XM_017004854.1:c.985G>T
|
XP_016860343.1:p.Ala329Ser
|
|
XR_001738924.1:n.929G>T
|
|
|
NM_001145664.2:c.646G>T
MANE Select
|
NP_001139136.2:p.Ala216Ser
|
|
NM_001367508.1:c.133G>T
|
NP_001354437.1:p.Ala45Ser
|
|
NM_001367509.1:c.133G>T
|
NP_001354438.1:p.Ala45Ser
|
|
NM_001367510.1:c.133G>T
|
NP_001354439.1:p.Ala45Ser
|
|