NM_199321.3:c.733T>G
MANE Select
|
NP_955353.1:p.Phe245Val
|
ENST00000348931.9:c.733T>G
MANE Select
|
ENSP00000335384.5:p.Phe245Val
|
NM_198844.2:c.667T>G
|
NP_942141.2:p.Phe223Val
|
NM_198844.3:c.667T>G
|
NP_942141.2:p.Phe223Val
|
NM_199321.2:c.733T>G
|
NP_955353.1:p.Phe245Val
|
ENST00000348931.8:c.733T>G
|
ENSP00000335384.5:p.Phe245Val
|
ENST00000377940.3:c.667T>G
|
ENSP00000367174.3:p.Phe223Val
|
ENST00000583811.5:c.379T>G
|
ENSP00000462463.1:p.Phe127Val
|
ENST00000584588.5:c.514T>G
|
ENSP00000462067.1:p.Phe172Val
|
XM_011524298.1:c.*9T>G
|
XP_011522600.1:n.*9T>G
|
XR_002957959.1:n.938T>G
|
|