ENST00000367408.6:n.3376C>A
|
|
|
ENST00000367409.9:c.10089C>A
MANE Select
|
ENSP00000356379.4:p.Asp3363Glu
|
|
ENST00000680265.1:c.10311C>A
|
ENSP00000505384.1:p.Asp3437Glu
|
|
ENST00000680710.1:c.10065C>A
|
ENSP00000506676.1:p.Asp3355Glu
|
|
ENST00000294732.11:c.5334C>A
|
ENSP00000294732.7:p.Asp1778Glu
|
|
ENST00000367408.5:c.3084C>A
|
ENSP00000356378.1:p.Asp1028Glu
|
|
ENST00000367409.8:c.10089C>A
|
ENSP00000356379.4:p.Asp3363Glu
|
|
ENST00000612785.1:c.4047C>A
|
ENSP00000479244.1:p.Asp1349Glu
|
|
NM_001206846.1:c.5334C>A
|
NP_001193775.1:p.Asp1778Glu
|
|
NM_018136.4:c.10089C>A
|
NP_060606.3:p.Asp3363Glu
|
|
NM_018136.5:c.10089C>A
MANE Select
|
NP_060606.3:p.Asp3363Glu
|
|
NM_001206846.2:c.5334C>A
|
NP_001193775.1:p.Asp1778Glu
|
|