ENST00000650793.2:n.569G>C
|
|
|
ENST00000697612.1:n.1247G>C
|
|
|
ENST00000374881.3:c.378G>C
|
ENSP00000364015.2:p.Leu126=
|
|
ENST00000374882.8:c.390G>C
MANE Select
|
ENSP00000364016.4:p.Leu130=
|
|
ENST00000650411.1:n.1711G>C
|
|
|
ENST00000650793.1:n.569G>C
|
|
|
ENST00000374881.2:c.378G>C
|
ENSP00000364015.2:p.Leu126=
|
|
ENST00000374882.7:c.390G>C
|
ENSP00000364016.3:p.Leu130=
|
|
ENST00000395339.7:c.318G>C
|
ENSP00000378748.3:p.Leu106=
|
|
ENST00000484003.1:n.774G>C
|
|
|
NM_004159.4:c.378G>C
|
NP_004150.1:p.Leu126=
|
|
NM_148919.3:c.390G>C
|
NP_683720.2:p.Leu130=
|
|
NM_148919.4:c.390G>C
MANE Select
|
NP_683720.2:p.Leu130=
|
|
NM_004159.5:c.378G>C
|
NP_004150.1:p.Leu126=
|
|