ENST00000443439.7:c.*1120C>A
(ERAP1)
MANE Select
|
ENSP00000406304.2:n.*1120C>A
|
|
ENST00000296754.7:c.2818+1128C>A
(ERAP1)
|
ENSP00000296754.3:n.2818+1128C>A
|
|
ENST00000443439.6:c.*1120C>A
(ERAP1)
|
ENSP00000406304.2:n.*1120C>A
|
|
ENST00000510098.1:c.963-1592G>T
(CAST)
|
ENSP00000427195.1:n.963-1592G>T
|
|
NM_001040458.1:c.*1120C>A
(ERAP1)
|
NP_001035548.1:n.*1120C>A
|
|
NM_001198541.1:c.*1120C>A
(ERAP1)
|
NP_001185470.1:n.*1120C>A
|
|
NM_016442.3:c.2818+1128C>A
(ERAP1)
|
NP_057526.3:n.2818+1128C>A
|
|
XM_005272015.3:c.2818+1128C>A
(ERAP1)
|
XP_005272072.1:n.2818+1128C>A
|
|
XM_005272016.3:c.2818+1128C>A
(ERAP1)
|
XP_005272073.1:n.2818+1128C>A
|
|
XM_011543480.1:c.2818+1128C>A
(ERAP1)
|
XP_011541782.1:n.2818+1128C>A
|
|
XM_011543481.1:c.2818+1128C>A
(ERAP1)
|
XP_011541783.1:n.2818+1128C>A
|
|
XM_011543482.1:c.2818+1128C>A
(ERAP1)
|
XP_011541784.1:n.2818+1128C>A
|
|
XM_011543483.1:c.2818+1128C>A
(ERAP1)
|
XP_011541785.1:n.2818+1128C>A
|
|
XM_011543484.1:c.2818+1128C>A
(ERAP1)
|
XP_011541786.1:n.2818+1128C>A
|
|
XM_011543485.1:c.2818+1128C>A
(ERAP1)
|
XP_011541787.1:n.2818+1128C>A
|
|
XM_011543486.1:c.*1120C>A
(ERAP1)
|
XP_011541788.1:n.*1120C>A
|
|
XM_011543487.1:c.2818+1128C>A
(ERAP1)
|
XP_011541789.1:n.2818+1128C>A
|
|
NM_001040458.2:c.*1120C>A
(ERAP1)
|
NP_001035548.1:n.*1120C>A
|
|
NM_001198541.2:c.*1120C>A
(ERAP1)
|
NP_001185470.1:n.*1120C>A
|
|
NM_001349244.1:c.2818+1128C>A
(ERAP1)
|
NP_001336173.1:n.2818+1128C>A
|
|
NM_016442.4:c.2818+1128C>A
(ERAP1)
|
NP_057526.3:n.2818+1128C>A
|
|
XM_005272015.5:c.2818+1128C>A
(ERAP1)
|
XP_005272072.1:n.2818+1128C>A
|
|
XM_005272016.4:c.2818+1128C>A
(ERAP1)
|
XP_005272073.1:n.2818+1128C>A
|
|
XM_011543480.2:c.2818+1128C>A
(ERAP1)
|
XP_011541782.1:n.2818+1128C>A
|
|
XM_011543481.2:c.2818+1128C>A
(ERAP1)
|
XP_011541783.1:n.2818+1128C>A
|
|
XM_011543484.2:c.2818+1128C>A
(ERAP1)
|
XP_011541786.1:n.2818+1128C>A
|
|
XM_011543485.2:c.2818+1128C>A
(ERAP1)
|
XP_011541787.1:n.2818+1128C>A
|
|
XM_011543486.3:c.*1120C>A
(ERAP1)
|
XP_011541788.1:n.*1120C>A
|
|
XM_017009581.1:c.2818+1128C>A
(ERAP1)
|
XP_016865070.1:n.2818+1128C>A
|
|
XM_017009583.2:c.1723+1128C>A
(ERAP1)
|
XP_016865072.1:n.1723+1128C>A
|
|
XM_024446113.1:c.2818+1128C>A
(ERAP1)
|
XP_024301881.1:n.2818+1128C>A
|
|
XR_001742119.2:n.2956+1128C>A
(ERAP1)
|
|
|
NM_001040458.3:c.*1120C>A
(ERAP1)
MANE Select
|
NP_001035548.1:n.*1120C>A
|
|
NM_001198541.3:c.*1120C>A
(ERAP1)
|
NP_001185470.1:n.*1120C>A
|
|
NM_001349244.2:c.2818+1128C>A
(ERAP1)
|
NP_001336173.1:n.2818+1128C>A
|
|
NM_016442.5:c.2818+1128C>A
(ERAP1)
|
NP_057526.3:n.2818+1128C>A
|
|