ENST00000650793.2:n.543G=
|
|
|
ENST00000697612.1:n.1221G=
|
|
|
ENST00000374881.3:c.352G=
|
ENSP00000364015.2:p.Ala118=
|
|
ENST00000374882.8:c.364G=
MANE Select
|
ENSP00000364016.4:p.Ala122=
|
|
ENST00000650411.1:n.1685G=
|
|
|
ENST00000650793.1:n.543G=
|
|
|
ENST00000374881.2:c.352G=
|
ENSP00000364015.2:p.Ala118=
|
|
ENST00000374882.7:c.364G=
|
ENSP00000364016.3:p.Ala122=
|
|
ENST00000395339.7:c.296-4G=
|
ENSP00000378748.3:n.296-4G=
|
|
ENST00000484003.1:n.748G=
|
|
|
NM_004159.4:c.352G=
|
NP_004150.1:p.Ala118=
|
|
NM_148919.3:c.364G=
|
NP_683720.2:p.Ala122=
|
|
NM_148919.4:c.364G=
MANE Select
|
NP_683720.2:p.Ala122=
|
|
NM_004159.5:c.352G=
|
NP_004150.1:p.Ala118=
|
|