ENST00000370274.8:c.709T>G
MANE Select
|
ENSP00000359297.3:p.Phe237Val
|
|
ENST00000370274.7:c.709T>G
|
ENSP00000359297.3:p.Phe237Val
|
|
ENST00000432467.1:c.709T>G
|
ENSP00000396266.1:p.Phe237Val
|
|
ENST00000440023.5:c.709T>G
|
ENSP00000391854.1:p.Phe237Val
|
|
NM_001129765.1:c.709T>G
|
NP_001123237.1:p.Phe237Val
|
|
NM_015922.2:c.709T>G
|
NP_057006.1:p.Phe237Val
|
|
XM_011531178.1:c.709T>G
|
XP_011529480.1:p.Phe237Val
|
|
XM_011531178.2:c.709T>G
|
XP_011529480.1:p.Phe237Val
|
|
XM_017029564.1:c.757T>G
|
XP_016885053.1:p.Phe253Val
|
|
NM_015922.3:c.709T>G
MANE Select
|
NP_057006.1:p.Phe237Val
|
|
NM_001129765.2:c.709T>G
|
NP_001123237.1:p.Phe237Val
|
|