ENST00000330342.8:c.1341T>C
MANE Select
|
ENSP00000332247.2:p.Phe447=
|
|
ENST00000540368.6:n.1372T>C
|
|
|
ENST00000674794.1:c.1429T>C
|
|
|
ENST00000675260.1:n.616T>C
|
|
|
ENST00000675344.1:c.*362T>C
|
ENSP00000501953.1:n.*362T>C
|
|
ENST00000330342.7:c.1341T>C
|
ENSP00000332247.2:p.Phe447=
|
|
ENST00000504192.2:c.951T>C
|
ENSP00000443441.1:p.Phe317=
|
|
ENST00000536426.1:n.358T>C
|
|
|
ENST00000545059.5:n.3977T>C
|
|
|
NM_012463.3:c.1341T>C
|
NP_036595.2:p.Phe447=
|
|
XM_005253563.1:c.1341T>C
|
XP_005253620.1:p.Phe447=
|
|
XM_006719317.2:c.828T>C
|
XP_006719380.1:p.Phe276=
|
|
XM_006719318.2:c.519T>C
|
XP_006719381.1:p.Phe173=
|
|
XR_429088.1:n.1504T>C
|
|
|
XM_024448910.1:c.1341T>C
|
XP_024304678.1:p.Phe447=
|
|
XM_024448911.1:c.828T>C
|
XP_024304679.1:p.Phe276=
|
|
XM_024448912.1:c.519T>C
|
XP_024304680.1:p.Phe173=
|
|
NM_012463.4:c.1341T>C
MANE Select
|
NP_036595.2:p.Phe447=
|
|