ENST00000650793.2:n.583G>A
|
|
|
ENST00000697612.1:n.1261G>A
|
|
|
ENST00000374881.3:c.392G>A
|
ENSP00000364015.2:p.Cys131Tyr
|
|
ENST00000374882.8:c.404G>A
MANE Select
|
ENSP00000364016.4:p.Cys135Tyr
|
|
ENST00000650411.1:n.1725G>A
|
|
|
ENST00000650793.1:n.583G>A
|
|
|
ENST00000374881.2:c.392G>A
|
ENSP00000364015.2:p.Cys131Tyr
|
|
ENST00000374882.7:c.404G>A
|
ENSP00000364016.3:p.Cys135Tyr
|
|
ENST00000395339.7:c.332G>A
|
ENSP00000378748.3:p.Cys111Tyr
|
|
ENST00000484003.1:n.788G>A
|
|
|
NM_004159.4:c.392G>A
|
NP_004150.1:p.Cys131Tyr
|
|
NM_148919.3:c.404G>A
|
NP_683720.2:p.Cys135Tyr
|
|
NM_148919.4:c.404G>A
MANE Select
|
NP_683720.2:p.Cys135Tyr
|
|
NM_004159.5:c.392G>A
|
NP_004150.1:p.Cys131Tyr
|
|