ENST00000650793.2:n.520T>A
|
|
|
ENST00000697612.1:n.1198T>A
|
|
|
ENST00000374881.3:c.329T>A
|
ENSP00000364015.2:p.Leu110His
|
|
ENST00000374882.8:c.341T>A
MANE Select
|
ENSP00000364016.4:p.Leu114His
|
|
ENST00000650411.1:n.1662T>A
|
|
|
ENST00000650793.1:n.520T>A
|
|
|
ENST00000374881.2:c.329T>A
|
ENSP00000364015.2:p.Leu110His
|
|
ENST00000374882.7:c.341T>A
|
ENSP00000364016.3:p.Leu114His
|
|
ENST00000395339.7:c.296-27T>A
|
ENSP00000378748.3:n.296-27T>A
|
|
ENST00000484003.1:n.725T>A
|
|
|
NM_004159.4:c.329T>A
|
NP_004150.1:p.Leu110His
|
|
NM_148919.3:c.341T>A
|
NP_683720.2:p.Leu114His
|
|
NM_148919.4:c.341T>A
MANE Select
|
NP_683720.2:p.Leu114His
|
|
NM_004159.5:c.329T>A
|
NP_004150.1:p.Leu110His
|
|