ENST00000330342.8:c.1378T>G
MANE Select
|
ENSP00000332247.2:p.Phe460Val
|
|
ENST00000540368.6:n.1409T>G
|
|
|
ENST00000674794.1:c.1466T>G
|
|
|
ENST00000675260.1:n.653T>G
|
|
|
ENST00000675344.1:c.*399T>G
|
ENSP00000501953.1:n.*399T>G
|
|
ENST00000330342.7:c.1378T>G
|
ENSP00000332247.2:p.Phe460Val
|
|
ENST00000536426.1:n.395T>G
|
|
|
ENST00000545059.5:n.4014T>G
|
|
|
NM_012463.3:c.1378T>G
|
NP_036595.2:p.Phe460Val
|
|
XM_005253563.1:c.1378T>G
|
XP_005253620.1:p.Phe460Val
|
|
XM_006719317.2:c.865T>G
|
XP_006719380.1:p.Phe289Val
|
|
XM_006719318.2:c.556T>G
|
XP_006719381.1:p.Phe186Val
|
|
XR_429088.1:n.1541T>G
|
|
|
XM_024448910.1:c.1378T>G
|
XP_024304678.1:p.Phe460Val
|
|
XM_024448911.1:c.865T>G
|
XP_024304679.1:p.Phe289Val
|
|
XM_024448912.1:c.556T>G
|
XP_024304680.1:p.Phe186Val
|
|
NM_012463.4:c.1378T>G
MANE Select
|
NP_036595.2:p.Phe460Val
|
|