ENST00000650793.2:n.563G=
|
|
|
ENST00000697612.1:n.1241G=
|
|
|
ENST00000374881.3:c.372G=
|
ENSP00000364015.2:p.Glu124=
|
|
ENST00000374882.8:c.384G=
MANE Select
|
ENSP00000364016.4:p.Glu128=
|
|
ENST00000650411.1:n.1705G=
|
|
|
ENST00000650793.1:n.563G=
|
|
|
ENST00000374881.2:c.372G=
|
ENSP00000364015.2:p.Glu124=
|
|
ENST00000374882.7:c.384G=
|
ENSP00000364016.3:p.Glu128=
|
|
ENST00000395339.7:c.312G=
|
ENSP00000378748.3:p.Glu104=
|
|
ENST00000484003.1:n.768G=
|
|
|
NM_004159.4:c.372G=
|
NP_004150.1:p.Glu124=
|
|
NM_148919.3:c.384G=
|
NP_683720.2:p.Glu128=
|
|
NM_148919.4:c.384G=
MANE Select
|
NP_683720.2:p.Glu128=
|
|
NM_004159.5:c.372G=
|
NP_004150.1:p.Glu124=
|
|