ENST00000324001.8:c.2097G=
MANE Select
|
ENSP00000326018.6:p.Met699=
|
|
ENST00000673881.1:c.1680G=
|
ENSP00000501070.1:p.Met560=
|
|
ENST00000674005.2:c.2382G=
|
ENSP00000501261.1:p.Met794=
|
|
ENST00000674773.1:c.1680G=
|
ENSP00000502579.1:p.Met560=
|
|
ENST00000675517.1:c.1972G=
|
|
|
ENST00000676076.1:c.1958G=
|
|
|
ENST00000676260.1:c.2059G=
|
|
|
ENST00000676316.1:c.1984G=
|
|
|
ENST00000291825.11:c.*2302G=
|
ENSP00000291825.6:n.*2302G=
|
|
ENST00000324001.7:c.2097G=
|
ENSP00000326018.6:p.Met699=
|
|
NM_020956.2:c.*2302G= , LRG_265t1:c.*2302G=
|
NP_066007.1:n.*2302G=
|
|
NM_181882.2:c.2097G= , LRG_265t2:c.2097G=
|
NP_870998.2:p.Met699=
|
|
XM_011527171.1:c.2097G=
|
XP_011525473.1:p.Met699=
|
|
XM_011527171.2:c.2097G=
|
XP_011525473.1:p.Met699=
|
|
XM_017027046.1:c.1995G=
|
XP_016882535.1:p.Met665=
|
|
XM_017027047.1:c.1995G=
|
XP_016882536.1:p.Met665=
|
|
NM_181882.3:c.2097G=
MANE Select
|
NP_870998.2:p.Met699=
|
|