ENST00000367408.6:n.2108-8681T>C
|
|
|
ENST00000367409.9:c.4406T>C
MANE Select
|
ENSP00000356379.4:p.Ile1469Thr
|
|
ENST00000680265.1:c.4406T>C
|
ENSP00000505384.1:p.Ile1469Thr
|
|
ENST00000680710.1:c.4406T>C
|
ENSP00000506676.1:p.Ile1469Thr
|
|
ENST00000681879.1:c.4454T>C
|
ENSP00000505363.1:n.4454T>C
|
|
ENST00000294732.11:c.4066-8681T>C
|
ENSP00000294732.7:n.4066-8681T>C
|
|
ENST00000367408.5:c.1816-8681T>C
|
ENSP00000356378.1:n.1816-8681T>C
|
|
ENST00000367409.8:c.4406T>C
|
ENSP00000356379.4:p.Ile1469Thr
|
|
ENST00000612785.1:c.562-2198T>C
|
ENSP00000479244.1:n.562-2198T>C
|
|
NM_001206846.1:c.4066-8681T>C
|
NP_001193775.1:n.4066-8681T>C
|
|
NM_018136.4:c.4406T>C
|
NP_060606.3:p.Ile1469Thr
|
|
NM_018136.5:c.4406T>C
MANE Select
|
NP_060606.3:p.Ile1469Thr
|
|
NM_001206846.2:c.4066-8681T>C
|
NP_001193775.1:n.4066-8681T>C
|
|