ENST00000322344.8:c.1126G>T
MANE Select
|
ENSP00000323511.2:p.Ala376Ser
|
|
ENST00000322344.7:c.1126G>T
|
ENSP00000323511.2:p.Ala376Ser
|
|
ENST00000593706.3:n.481G>T
|
|
|
ENST00000593946.5:c.*1053G>T
|
ENSP00000468896.1:n.*1053G>T
|
|
ENST00000594661.5:n.1627G>T
|
|
|
ENST00000596014.5:c.1126G>T
|
ENSP00000472300.1:p.Ala376Ser
|
|
ENST00000600573.5:c.1033G>T
|
ENSP00000469826.1:p.Ala345Ser
|
|
ENST00000600910.5:c.1126G>T
|
ENSP00000473137.1:p.Ala376Ser
|
|
ENST00000601816.3:n.25G>T
|
|
|
ENST00000625216.2:c.208-80G>T
|
ENSP00000486898.1:n.208-80G>T
|
|
ENST00000627232.2:c.1046G>T
|
ENSP00000486037.1:n.1046G>T
|
|
ENST00000627317.1:c.747G>T
|
|
|
ENST00000631020.2:c.1018G>T
|
ENSP00000486707.1:p.Ala340Ser
|
|
NM_007254.3:c.1126G>T
|
NP_009185.2:p.Ala376Ser
|
|
NM_007254.4:c.1126G>T
MANE Select
|
NP_009185.2:p.Ala376Ser
|
|