ENST00000352511.5:c.1273G>C
MANE Select
|
ENSP00000340361.3:p.Glu425Gln
|
|
ENST00000352511.4:c.1273G>C
|
ENSP00000340361.3:p.Glu425Gln
|
|
ENST00000461232.1:n.5062G>C
|
|
|
ENST00000465020.5:n.1359G>C
|
|
|
NM_001106.3:c.1273G>C
|
NP_001097.2:p.Glu425Gln
|
|
XM_005265583.2:c.1336G>C
|
XP_005265640.1:p.Glu446Gln
|
|
XM_005265583.3:c.1336G>C
|
XP_005265640.1:p.Glu446Gln
|
|
XM_017007514.1:c.1315G>C
|
XP_016863003.1:p.Glu439Gln
|
|
XM_017007515.2:c.1291G>C
|
XP_016863004.1:p.Glu431Gln
|
|
XM_017007516.1:c.1270G>C
|
XP_016863005.1:p.Glu424Gln
|
|
NM_001106.4:c.1273G>C
MANE Select
|
NP_001097.2:p.Glu425Gln
|
|