ENST00000367408.6:n.3121A>C
|
|
|
ENST00000367409.9:c.9834A>C
MANE Select
|
ENSP00000356379.4:p.Val3278=
|
|
ENST00000680265.1:c.10056A>C
|
ENSP00000505384.1:p.Val3352=
|
|
ENST00000680710.1:c.9810A>C
|
ENSP00000506676.1:p.Val3270=
|
|
ENST00000294732.11:c.5079A>C
|
ENSP00000294732.7:p.Val1693=
|
|
ENST00000367408.5:c.2829A>C
|
ENSP00000356378.1:p.Val943=
|
|
ENST00000367409.8:c.9834A>C
|
ENSP00000356379.4:p.Val3278=
|
|
ENST00000612785.1:c.3792A>C
|
ENSP00000479244.1:p.Val1264=
|
|
NM_001206846.1:c.5079A>C
|
NP_001193775.1:p.Val1693=
|
|
NM_018136.4:c.9834A>C
|
NP_060606.3:p.Val3278=
|
|
NM_018136.5:c.9834A>C
MANE Select
|
NP_060606.3:p.Val3278=
|
|
NM_001206846.2:c.5079A>C
|
NP_001193775.1:p.Val1693=
|
|