ENST00000367408.6:n.3280A>G
|
|
|
ENST00000367409.9:c.9993A>G
MANE Select
|
ENSP00000356379.4:p.Lys3331=
|
|
ENST00000680265.1:c.10215A>G
|
ENSP00000505384.1:p.Lys3405=
|
|
ENST00000680710.1:c.9969A>G
|
ENSP00000506676.1:p.Lys3323=
|
|
ENST00000294732.11:c.5238A>G
|
ENSP00000294732.7:p.Lys1746=
|
|
ENST00000367408.5:c.2988A>G
|
ENSP00000356378.1:p.Lys996=
|
|
ENST00000367409.8:c.9993A>G
|
ENSP00000356379.4:p.Lys3331=
|
|
ENST00000612785.1:c.3951A>G
|
ENSP00000479244.1:p.Lys1317=
|
|
NM_001206846.1:c.5238A>G
|
NP_001193775.1:p.Lys1746=
|
|
NM_018136.4:c.9993A>G
|
NP_060606.3:p.Lys3331=
|
|
NM_018136.5:c.9993A>G
MANE Select
|
NP_060606.3:p.Lys3331=
|
|
NM_001206846.2:c.5238A>G
|
NP_001193775.1:p.Lys1746=
|
|