ENST00000350026.11:c.3886A=
|
ENSP00000055163.8:p.Met1296=
|
|
ENST00000414678.8:c.3955A=
|
ENSP00000412835.3:p.Met1319=
|
|
ENST00000637015.2:c.4174A=
|
ENSP00000489729.2:p.Met1392=
|
|
ENST00000346085.10:c.3925A=
|
ENSP00000344546.5:p.Met1309=
|
|
ENST00000350026.10:c.3637A=
|
ENSP00000055163.7:p.Met1213=
|
|
ENST00000414678.7:c.2203A=
|
ENSP00000412835.2:p.Met735=
|
|
ENST00000635849.1:c.1366A=
|
ENSP00000490948.1:p.Met456=
|
|
ENST00000635957.1:c.1000A=
|
ENSP00000490385.1:p.Met334=
|
|
ENST00000636930.2:c.4045A=
MANE Select
|
ENSP00000490491.2:p.Met1349=
|
|
ENST00000636940.1:n.2042A=
|
|
|
ENST00000637015.1:c.1413A=
|
|
|
ENST00000637568.1:c.1327A=
|
|
|
ENST00000637741.1:n.711A=
|
|
|
ENST00000637810.1:c.1387A=
|
ENSP00000489636.1:p.Met463=
|
|
ENST00000637904.1:c.1546A=
|
ENSP00000490550.1:p.Met516=
|
|
ENST00000647938.1:c.3676A=
|
ENSP00000498155.1:p.Met1226=
|
|
ENST00000346085.9:c.3676A=
|
ENSP00000344546.4:p.Met1226=
|
|
ENST00000350026.9:c.3637A=
|
ENSP00000055163.7:p.Met1213=
|
|
ENST00000414678.6:c.2203A=
|
ENSP00000412835.2:p.Met735=
|
|
NM_017519.2:c.3637A=
|
NP_059989.2:p.Met1213=
|
|
NM_020732.3:c.3676A=
|
NP_065783.3:p.Met1226=
|
|
XM_005267069.3:c.3796A=
|
XP_005267126.2:p.Met1266=
|
|
XM_011535984.1:c.2875A=
|
XP_011534286.1:p.Met959=
|
|
XM_011535985.1:c.2695A=
|
XP_011534287.1:p.Met899=
|
|
XM_011535986.1:c.2455A=
|
XP_011534288.1:p.Met819=
|
|
XM_011535987.1:c.2074A=
|
XP_011534289.1:p.Met692=
|
|
XM_011535988.1:c.937A=
|
XP_011534290.1:p.Met313=
|
|
NM_001346813.1:c.3796A=
|
NP_001333742.1:p.Met1266=
|
|
NM_001363725.1:c.1546A=
|
NP_001350654.1:p.Met516=
|
|
XM_011535984.2:c.4006A=
|
XP_011534286.2:p.Met1336=
|
|
XM_011535988.3:c.937A=
|
XP_011534290.1:p.Met313=
|
|
XM_017011103.2:c.3907A=
|
XP_016866592.1:p.Met1303=
|
|
XM_017011104.1:c.3877A=
|
XP_016866593.1:p.Met1293=
|
|
XM_017011105.2:c.3847A=
|
XP_016866594.1:p.Met1283=
|
|
XM_017011106.2:c.3718A=
|
XP_016866595.1:p.Met1240=
|
|
XM_017011107.2:c.3697A=
|
XP_016866596.1:p.Met1233=
|
|
XR_002956289.1:n.4089A=
|
|
|
NM_001363725.2:c.1546A=
|
NP_001350654.1:p.Met516=
|
|
NM_001371656.1:c.3925A=
|
NP_001358585.1:p.Met1309=
|
|
NM_001374820.1:c.3925A=
|
NP_001361749.1:p.Met1309=
|
|
NM_001374828.1:c.4045A=
MANE Select
|
NP_001361757.1:p.Met1349=
|
|
NM_017519.3:c.3886A=
|
NP_059989.3:p.Met1296=
|
|