ENST00000330342.8:c.1162G>T
MANE Select
|
ENSP00000332247.2:p.Val388Phe
|
|
ENST00000540368.6:n.1193G>T
|
|
|
ENST00000674794.1:c.1250G>T
|
|
|
ENST00000675260.1:n.437G>T
|
|
|
ENST00000675344.1:c.*183G>T
|
ENSP00000501953.1:n.*183G>T
|
|
ENST00000330342.7:c.1162G>T
|
ENSP00000332247.2:p.Val388Phe
|
|
ENST00000504192.2:c.772G>T
|
ENSP00000443441.1:p.Val258Phe
|
|
ENST00000536426.1:n.179G>T
|
|
|
ENST00000545059.5:n.3798G>T
|
|
|
NM_012463.3:c.1162G>T
|
NP_036595.2:p.Val388Phe
|
|
XM_005253563.1:c.1162G>T
|
XP_005253620.1:p.Val388Phe
|
|
XM_006719317.2:c.649G>T
|
XP_006719380.1:p.Val217Phe
|
|
XM_006719318.2:c.340G>T
|
XP_006719381.1:p.Val114Phe
|
|
XR_429088.1:n.1325G>T
|
|
|
XM_024448910.1:c.1162G>T
|
XP_024304678.1:p.Val388Phe
|
|
XM_024448911.1:c.649G>T
|
XP_024304679.1:p.Val217Phe
|
|
XM_024448912.1:c.340G>T
|
XP_024304680.1:p.Val114Phe
|
|
NM_012463.4:c.1162G>T
MANE Select
|
NP_036595.2:p.Val388Phe
|
|