ENST00000367590.9:c.276G>C
MANE Select
|
ENSP00000356562.4:p.Gln92His
|
|
ENST00000367589.3:c.276G>C
|
ENSP00000356561.3:p.Gln92His
|
|
ENST00000367590.8:c.276G>C
|
ENSP00000356562.4:p.Gln92His
|
|
NM_001135669.1:c.276G>C
|
NP_001129141.1:p.Gln92His
|
|
NM_004736.3:c.276G>C
|
NP_004727.2:p.Gln92His
|
|
NM_001328662.1:c.276G>C
|
NP_001315591.1:p.Gln92His
|
|
NR_137330.1:n.468G>C
|
|
|
NM_001135669.2:c.276G>C
|
NP_001129141.1:p.Gln92His
|
|
NM_001328662.2:c.276G>C
|
NP_001315591.1:p.Gln92His
|
|
NM_004736.4:c.276G>C
MANE Select
|
NP_004727.2:p.Gln92His
|
|
NR_137330.2:n.456G>C
|
|
|