ENST00000342947.9:c.521T=
|
ENSP00000339587.3:p.Met174=
|
|
ENST00000409970.6:c.29T=
|
ENSP00000387119.1:p.Met10=
|
|
ENST00000411476.3:n.290T=
|
|
|
ENST00000414428.2:c.521T=
|
ENSP00000413963.2:p.Met174=
|
|
ENST00000419307.6:c.29T=
|
ENSP00000401332.1:p.Met10=
|
|
ENST00000559637.6:n.216T=
|
|
|
ENST00000645220.1:c.521T=
MANE Select
|
ENSP00000494186.1:p.Met174=
|
|
ENST00000342947.7:c.521T=
|
ENSP00000339587.3:p.Met174=
|
|
ENST00000409775.7:c.521T=
|
ENSP00000386670.3:p.Met174=
|
|
ENST00000409970.5:c.29T=
|
ENSP00000387119.1:p.Met10=
|
|
ENST00000411476.2:c.290T=
|
ENSP00000414090.2:p.Met97=
|
|
ENST00000414428.1:c.29T=
|
ENSP00000413963.1:p.Met10=
|
|
ENST00000419307.5:c.29T=
|
ENSP00000401332.1:p.Met10=
|
|
ENST00000493723.5:n.540T=
|
|
|
ENST00000559637.5:n.216T=
|
|
|
NM_001127453.1:c.521T=
|
NP_001120925.1:p.Met174=
|
|
NM_001127454.1:c.29T=
|
NP_001120926.1:p.Met10=
|
|
NM_004403.2:c.521T=
|
NP_004394.1:p.Met174=
|
|
XM_017011802.1:c.29T=
|
XP_016867291.1:p.Met10=
|
|
XM_024446670.1:c.521T=
|
XP_024302438.1:p.Met174=
|
|
NM_004403.3:c.521T=
|
NP_004394.1:p.Met174=
|
|
NM_001127453.2:c.521T=
MANE Select
|
NP_001120925.1:p.Met174=
|
|
NM_001127454.2:c.29T=
|
NP_001120926.1:p.Met10=
|
|