ENST00000330342.8:c.1146C>T
MANE Select
|
ENSP00000332247.2:p.Ile382=
|
|
ENST00000540368.6:n.1177C>T
|
|
|
ENST00000674794.1:c.1234C>T
|
|
|
ENST00000675260.1:n.421C>T
|
|
|
ENST00000675344.1:c.*167C>T
|
ENSP00000501953.1:n.*167C>T
|
|
ENST00000330342.7:c.1146C>T
|
ENSP00000332247.2:p.Ile382=
|
|
ENST00000504192.2:c.756C>T
|
ENSP00000443441.1:p.Ile252=
|
|
ENST00000536426.1:n.163C>T
|
|
|
ENST00000545059.5:n.3782C>T
|
|
|
NM_012463.3:c.1146C>T
|
NP_036595.2:p.Ile382=
|
|
XM_005253563.1:c.1146C>T
|
XP_005253620.1:p.Ile382=
|
|
XM_006719317.2:c.633C>T
|
XP_006719380.1:p.Ile211=
|
|
XM_006719318.2:c.324C>T
|
XP_006719381.1:p.Ile108=
|
|
XR_429088.1:n.1309C>T
|
|
|
XM_024448910.1:c.1146C>T
|
XP_024304678.1:p.Ile382=
|
|
XM_024448911.1:c.633C>T
|
XP_024304679.1:p.Ile211=
|
|
XM_024448912.1:c.324C>T
|
XP_024304680.1:p.Ile108=
|
|
NM_012463.4:c.1146C>T
MANE Select
|
NP_036595.2:p.Ile382=
|
|