ENST00000650793.2:n.557C>T
|
|
|
ENST00000697612.1:n.1235C>T
|
|
|
ENST00000374881.3:c.366C>T
|
ENSP00000364015.2:p.Tyr122=
|
|
ENST00000374882.8:c.378C>T
MANE Select
|
ENSP00000364016.4:p.Tyr126=
|
|
ENST00000650411.1:n.1699C>T
|
|
|
ENST00000650793.1:n.557C>T
|
|
|
ENST00000374881.2:c.366C>T
|
ENSP00000364015.2:p.Tyr122=
|
|
ENST00000374882.7:c.378C>T
|
ENSP00000364016.3:p.Tyr126=
|
|
ENST00000395339.7:c.306C>T
|
ENSP00000378748.3:p.Tyr102=
|
|
ENST00000484003.1:n.762C>T
|
|
|
NM_004159.4:c.366C>T
|
NP_004150.1:p.Tyr122=
|
|
NM_148919.3:c.378C>T
|
NP_683720.2:p.Tyr126=
|
|
NM_148919.4:c.378C>T
MANE Select
|
NP_683720.2:p.Tyr126=
|
|
NM_004159.5:c.366C>T
|
NP_004150.1:p.Tyr122=
|
|