ENST00000261769.10:c.2008A=
MANE Select
|
ENSP00000261769.4:p.Met670=
|
|
ENST00000261769.9:c.2008A=
|
ENSP00000261769.4:p.Met670=
|
|
ENST00000422392.6:c.1825A=
|
ENSP00000414946.2:p.Met609=
|
|
ENST00000562118.1:n.226A=
|
|
|
ENST00000562836.5:n.2079A=
|
|
|
ENST00000566510.5:c.*674A=
|
ENSP00000458139.1:n.*674A=
|
|
ENST00000566612.5:c.*248A=
|
ENSP00000454782.1:n.*248A=
|
|
ENST00000611625.4:c.2071A=
|
ENSP00000481063.1:p.Met691=
|
|
ENST00000612417.4:c.1830+1351A=
|
ENSP00000478360.1:n.1830+1351A=
|
|
ENST00000621016.4:c.1865+1316A=
|
ENSP00000480664.1:n.1865+1316A=
|
|
NM_004360.3:c.2008A= , LRG_301t1:c.2008A=
|
NP_004351.1:p.Met670=
|
|
XM_011523488.1:c.1273A=
|
XP_011521790.1:p.Met425=
|
|
XM_011523489.1:c.1273A=
|
XP_011521791.1:p.Met425=
|
|
NM_001317184.1:c.1825A=
|
NP_001304113.1:p.Met609=
|
|
NM_001317185.1:c.460A=
|
NP_001304114.1:p.Met154=
|
|
NM_001317186.1:c.43A=
|
NP_001304115.1:p.Met15=
|
|
NM_004360.4:c.2008A=
|
NP_004351.1:p.Met670=
|
|
NM_004360.5:c.2008A=
MANE Select
|
NP_004351.1:p.Met670=
|
|
NM_001317184.2:c.1825A=
|
NP_001304113.1:p.Met609=
|
|
NM_001317185.2:c.460A=
|
NP_001304114.1:p.Met154=
|
|
NM_001317186.2:c.43A=
|
NP_001304115.1:p.Met15=
|
|