ENST00000263791.10:c.4188T>A
MANE Select
|
ENSP00000263791.5:p.Ser1396=
|
|
ENST00000263791.9:c.4188T>A
|
ENSP00000263791.5:p.Ser1396=
|
|
ENST00000558557.1:n.1180T>A
|
|
|
ENST00000558629.5:n.3105T>A
|
|
|
ENST00000558743.1:n.388T>A
|
|
|
ENST00000560855.5:c.3520T>A
|
|
|
NM_001013703.3:c.4188T>A
|
NP_001013725.2:p.Ser1396=
|
|
XM_005254392.1:c.4188T>A
|
XP_005254449.1:p.Ser1396=
|
|
XM_011521599.1:c.4188T>A
|
XP_011519901.1:p.Ser1396=
|
|
XM_011521600.1:c.4017T>A
|
XP_011519902.1:p.Ser1339=
|
|
XM_005254392.3:c.4188T>A
|
XP_005254449.1:p.Ser1396=
|
|
XM_011521599.2:c.4188T>A
|
XP_011519901.1:p.Ser1396=
|
|
XM_011521600.3:c.4017T>A
|
XP_011519902.1:p.Ser1339=
|
|
XM_017022219.2:c.4017T>A
|
XP_016877708.1:p.Ser1339=
|
|
NM_001013703.4:c.4188T>A
MANE Select
|
NP_001013725.2:p.Ser1396=
|
|