ENST00000356392.9:c.1132T>G
MANE Select
|
ENSP00000348757.3:p.Phe378Val
|
|
ENST00000356392.8:c.1132T>G
|
ENSP00000348757.3:p.Phe378Val
|
|
ENST00000586836.5:c.559T>G
|
ENSP00000467429.1:p.Phe187Val
|
|
ENST00000591179.5:c.952T>G
|
ENSP00000466800.1:p.Phe318Val
|
|
ENST00000591345.5:c.*1051T>G
|
ENSP00000467313.1:n.*1051T>G
|
|
NM_001302453.1:c.970T>G
|
NP_001289382.1:p.Phe324Val
|
|
NM_001302454.1:c.952T>G
|
NP_001289383.1:p.Phe318Val
|
|
NM_145045.4:c.1132T>G
|
NP_659482.3:p.Phe378Val
|
|
XM_017026241.1:c.*26T>G
|
XP_016881730.1:n.*26T>G
|
|
NM_145045.5:c.1132T>G
MANE Select
|
NP_659482.3:p.Phe378Val
|
|
NM_001302454.2:c.952T>G
|
NP_001289383.1:p.Phe318Val
|
|