ENST00000330342.8:c.851T>A
MANE Select
|
ENSP00000332247.2:p.Leu284Ter
|
|
ENST00000540368.6:n.882T>A
|
|
|
ENST00000613625.5:c.851T>A
|
ENSP00000482236.1:p.Leu284Ter
|
|
ENST00000674794.1:c.939T>A
|
|
|
ENST00000675344.1:c.851T>A
|
ENSP00000501953.1:p.Leu284Ter
|
|
ENST00000330342.7:c.851T>A
|
ENSP00000332247.2:p.Leu284Ter
|
|
ENST00000504192.2:c.461T>A
|
ENSP00000443441.1:p.Leu154Ter
|
|
ENST00000540368.5:n.1061T>A
|
|
|
ENST00000545059.5:n.3487T>A
|
|
|
ENST00000613625.4:c.851T>A
|
ENSP00000482236.1:p.Leu284Ter
|
|
NM_012463.3:c.851T>A
|
NP_036595.2:p.Leu284Ter
|
|
XM_005253563.1:c.851T>A
|
XP_005253620.1:p.Leu284Ter
|
|
XM_006719317.2:c.338T>A
|
XP_006719380.1:p.Leu113Ter
|
|
XM_006719318.2:c.29T>A
|
XP_006719381.1:p.Leu10Ter
|
|
XR_429088.1:n.1014T>A
|
|
|
XM_024448910.1:c.851T>A
|
XP_024304678.1:p.Leu284Ter
|
|
XM_024448911.1:c.338T>A
|
XP_024304679.1:p.Leu113Ter
|
|
XM_024448912.1:c.29T>A
|
XP_024304680.1:p.Leu10Ter
|
|
NM_012463.4:c.851T>A
MANE Select
|
NP_036595.2:p.Leu284Ter
|
|