ENST00000367409.9:c.876G>C
MANE Select
|
ENSP00000356379.4:p.Glu292Asp
|
|
ENST00000679766.1:n.1093G>C
|
|
|
ENST00000680265.1:c.876G>C
|
ENSP00000505384.1:p.Glu292Asp
|
|
ENST00000680710.1:c.876G>C
|
ENSP00000506676.1:p.Glu292Asp
|
|
ENST00000681879.1:c.876G>C
|
ENSP00000505363.1:p.Glu292Asp
|
|
ENST00000294732.11:c.876G>C
|
ENSP00000294732.7:p.Glu292Asp
|
|
ENST00000367409.8:c.876G>C
|
ENSP00000356379.4:p.Glu292Asp
|
|
ENST00000612785.1:c.561+315G>C
|
ENSP00000479244.1:n.561+315G>C
|
|
NM_001206846.1:c.876G>C
|
NP_001193775.1:p.Glu292Asp
|
|
NM_018136.4:c.876G>C
|
NP_060606.3:p.Glu292Asp
|
|
NM_018136.5:c.876G>C
MANE Select
|
NP_060606.3:p.Glu292Asp
|
|
NM_001206846.2:c.876G>C
|
NP_001193775.1:p.Glu292Asp
|
|