ENST00000283871.10:c.575T>G
MANE Select
|
ENSP00000283871.5:p.Val192Gly
|
|
ENST00000283871.9:c.575T>G
|
ENSP00000283871.5:p.Val192Gly
|
|
ENST00000475447.2:c.106T>G
|
|
|
ENST00000492108.5:c.180+632T>G
|
ENSP00000419838.1:n.180+632T>G
|
|
NM_000187.3:c.575T>G
|
NP_000178.2:p.Val192Gly
|
|
XM_005247412.1:c.549+632T>G
|
XP_005247469.1:n.549+632T>G
|
|
XM_005247413.1:c.575T>G
|
XP_005247470.1:p.Val192Gly
|
|
XM_005247414.3:c.575T>G
|
XP_005247471.1:p.Val192Gly
|
|
XM_011512746.1:c.575T>G
|
XP_011511048.1:p.Val192Gly
|
|
XM_005247412.2:c.549+632T>G
|
XP_005247469.1:n.549+632T>G
|
|
XM_005247413.2:c.575T>G
|
XP_005247470.1:p.Val192Gly
|
|
XM_005247414.5:c.575T>G
|
XP_005247471.1:p.Val192Gly
|
|
XM_011512746.2:c.575T>G
|
XP_011511048.1:p.Val192Gly
|
|
XM_017006277.2:c.152T>G
|
XP_016861766.1:p.Val51Gly
|
|
NM_000187.4:c.575T>G
MANE Select
|
NP_000178.2:p.Val192Gly
|
|