ENST00000650793.2:n.560G>A
|
|
|
ENST00000697612.1:n.1238G>A
|
|
|
ENST00000374881.3:c.369G>A
|
ENSP00000364015.2:p.Trp123Ter
|
|
ENST00000374882.8:c.381G>A
MANE Select
|
ENSP00000364016.4:p.Trp127Ter
|
|
ENST00000650411.1:n.1702G>A
|
|
|
ENST00000650793.1:n.560G>A
|
|
|
ENST00000374881.2:c.369G>A
|
ENSP00000364015.2:p.Trp123Ter
|
|
ENST00000374882.7:c.381G>A
|
ENSP00000364016.3:p.Trp127Ter
|
|
ENST00000395339.7:c.309G>A
|
ENSP00000378748.3:p.Trp103Ter
|
|
ENST00000484003.1:n.765G>A
|
|
|
NM_004159.4:c.369G>A
|
NP_004150.1:p.Trp123Ter
|
|
NM_148919.3:c.381G>A
|
NP_683720.2:p.Trp127Ter
|
|
NM_148919.4:c.381G>A
MANE Select
|
NP_683720.2:p.Trp127Ter
|
|
NM_004159.5:c.369G>A
|
NP_004150.1:p.Trp123Ter
|
|