ENST00000399744.8:c.273G>C
MANE Select
|
ENSP00000382648.4:p.Gln91His
|
|
ENST00000474897.6:c.273G>C
|
ENSP00000434235.2:p.Gln91His
|
|
ENST00000329627.11:c.273G>C
|
ENSP00000331106.5:p.Gln91His
|
|
ENST00000399744.7:c.273G>C
|
ENSP00000382648.3:p.Gln91His
|
|
ENST00000428061.2:c.273G>C
|
ENSP00000412441.2:p.Gln91His
|
|
ENST00000474897.5:c.273G>C
|
ENSP00000434235.1:p.Gln91His
|
|
ENST00000610387.4:c.273G>C
|
ENSP00000482091.1:p.Gln91His
|
|
NM_001127649.2:c.273G>C
|
NP_001121121.1:p.Gln91His
|
|
NM_001199319.1:c.273G>C
|
NP_001186248.1:p.Gln91His
|
|
NM_017929.5:c.273G>C
|
NP_060399.1:p.Gln91His
|
|
NM_001127649.3:c.273G>C
MANE Select
|
NP_001121121.1:p.Gln91His
|
|
NM_001199319.2:c.273G>C
|
NP_001186248.1:p.Gln91His
|
|
NM_017929.6:c.273G>C
|
NP_060399.1:p.Gln91His
|
|