ENST00000367408.6:n.3436A>G
|
|
|
ENST00000367409.9:c.10149A>G
MANE Select
|
ENSP00000356379.4:p.Thr3383=
|
|
ENST00000680265.1:c.10371A>G
|
ENSP00000505384.1:p.Thr3457=
|
|
ENST00000680710.1:c.10125A>G
|
ENSP00000506676.1:p.Thr3375=
|
|
ENST00000294732.11:c.5394A>G
|
ENSP00000294732.7:p.Thr1798=
|
|
ENST00000367408.5:c.3144A>G
|
ENSP00000356378.1:p.Thr1048=
|
|
ENST00000367409.8:c.10149A>G
|
ENSP00000356379.4:p.Thr3383=
|
|
ENST00000612785.1:c.4107A>G
|
ENSP00000479244.1:p.Thr1369=
|
|
NM_001206846.1:c.5394A>G
|
NP_001193775.1:p.Thr1798=
|
|
NM_018136.4:c.10149A>G
|
NP_060606.3:p.Thr3383=
|
|
NM_018136.5:c.10149A>G
MANE Select
|
NP_060606.3:p.Thr3383=
|
|
NM_001206846.2:c.5394A>G
|
NP_001193775.1:p.Thr1798=
|
|