ENST00000650793.2:n.571T=
|
|
|
ENST00000697612.1:n.1249T=
|
|
|
ENST00000374881.3:c.380T=
|
ENSP00000364015.2:p.Leu127=
|
|
ENST00000374882.8:c.392T=
MANE Select
|
ENSP00000364016.4:p.Leu131=
|
|
ENST00000650411.1:n.1713T=
|
|
|
ENST00000650793.1:n.571T=
|
|
|
ENST00000374881.2:c.380T=
|
ENSP00000364015.2:p.Leu127=
|
|
ENST00000374882.7:c.392T=
|
ENSP00000364016.3:p.Leu131=
|
|
ENST00000395339.7:c.320T=
|
ENSP00000378748.3:p.Leu107=
|
|
ENST00000484003.1:n.776T=
|
|
|
NM_004159.4:c.380T=
|
NP_004150.1:p.Leu127=
|
|
NM_148919.3:c.392T=
|
NP_683720.2:p.Leu131=
|
|
NM_148919.4:c.392T=
MANE Select
|
NP_683720.2:p.Leu131=
|
|
NM_004159.5:c.380T=
|
NP_004150.1:p.Leu127=
|
|