ENST00000356608.7:c.4042A>G
MANE Select
|
ENSP00000349017.2:p.Met1348Val
|
|
ENST00000353782.9:c.3928A>G
|
ENSP00000311326.6:p.Met1310Val
|
|
ENST00000356608.6:c.4042A>G
|
ENSP00000349017.2:p.Met1348Val
|
|
ENST00000394747.5:c.4042A>G
|
ENSP00000378230.1:p.Met1348Val
|
|
ENST00000394748.5:c.4042A>G
|
ENSP00000378231.1:p.Met1348Val
|
|
ENST00000565329.1:n.1342A>G
|
|
|
NM_032583.3:c.4042A>G
|
NP_115972.2:p.Met1348Val
|
|
NM_033151.3:c.4042A>G
|
NP_149163.2:p.Met1348Val
|
|
NM_145186.2:c.3928A>G
|
NP_660187.1:p.Met1310Val
|
|
XM_011523396.1:c.3844A>G
|
XP_011521698.1:p.Met1282Val
|
|
XM_011523397.1:c.3085A>G
|
XP_011521699.1:p.Met1029Val
|
|
XM_011523398.1:c.2173A>G
|
XP_011521700.1:p.Met725Val
|
|
XM_011523397.2:c.3085A>G
|
XP_011521699.1:p.Met1029Val
|
|
XM_011523398.3:c.2173A>G
|
XP_011521700.1:p.Met725Val
|
|
XM_017023795.2:c.4042A>G
|
XP_016879284.1:p.Met1348Val
|
|
XM_017023796.2:c.4042A>G
|
XP_016879285.1:p.Met1348Val
|
|
XM_017023797.2:c.4042A>G
|
XP_016879286.1:p.Met1348Val
|
|
XM_017023798.2:c.4042A>G
|
XP_016879287.1:p.Met1348Val
|
|
XM_017023799.2:c.4042A>G
|
XP_016879288.1:p.Met1348Val
|
|
XM_017023800.2:c.4042A>G
|
XP_016879289.1:p.Met1348Val
|
|
XM_017023801.2:c.3934A>G
|
XP_016879290.1:p.Met1312Val
|
|
XM_017023802.2:c.3085A>G
|
XP_016879291.1:p.Met1029Val
|
|
XM_024450475.1:c.3085A>G
|
XP_024306243.1:p.Met1029Val
|
|
XR_001752012.1:n.6720A>G
|
|
|
NM_001370496.1:c.4048A>G
|
NP_001357425.1:p.Met1350Val
|
|
NM_001370497.1:c.4042A>G
MANE Select
|
NP_001357426.1:p.Met1348Val
|
|
NM_032583.4:c.4042A>G
|
NP_115972.2:p.Met1348Val
|
|
NM_033151.4:c.4042A>G
|
NP_149163.2:p.Met1348Val
|
|
NM_145186.3:c.3928A>G
|
NP_660187.1:p.Met1310Val
|
|