ENST00000283871.10:c.985T>G
MANE Select
|
ENSP00000283871.5:p.Phe329Val
|
|
ENST00000283871.9:c.985T>G
|
ENSP00000283871.5:p.Phe329Val
|
|
ENST00000470321.1:n.325T>G
|
|
|
ENST00000475447.2:c.307+3113T>G
|
|
|
ENST00000492108.5:c.285+3113T>G
|
ENSP00000419838.1:n.285+3113T>G
|
|
ENST00000494453.1:c.405T>G
|
|
|
NM_000187.3:c.985T>G
|
NP_000178.2:p.Phe329Val
|
|
XM_005247412.1:c.760T>G
|
XP_005247469.1:p.Phe254Val
|
|
XM_005247413.1:c.985T>G
|
XP_005247470.1:p.Phe329Val
|
|
XM_011512746.1:c.879+3113T>G
|
XP_011511048.1:n.879+3113T>G
|
|
XM_005247412.2:c.760T>G
|
XP_005247469.1:p.Phe254Val
|
|
XM_005247413.2:c.985T>G
|
XP_005247470.1:p.Phe329Val
|
|
XM_011512746.2:c.879+3113T>G
|
XP_011511048.1:n.879+3113T>G
|
|
XM_017006277.2:c.562T>G
|
XP_016861766.1:p.Phe188Val
|
|
NM_000187.4:c.985T>G
MANE Select
|
NP_000178.2:p.Phe329Val
|
|