ENST00000460680.6:c.2061G=
MANE Select
|
ENSP00000417132.1:p.Met687=
|
|
ENST00000296288.9:c.2007G=
|
ENSP00000296288.5:p.Met669=
|
|
ENST00000460680.5:c.2061G=
|
ENSP00000417132.1:p.Met687=
|
|
ENST00000466093.1:n.734G=
|
|
|
ENST00000469613.5:c.260G=
|
|
|
ENST00000478368.1:c.633G=
|
ENSP00000420647.1:p.Met211=
|
|
NM_004656.3:c.2061G=
|
NP_004647.1:p.Met687=
|
|
XM_011534149.1:c.2130G=
|
XP_011532451.1:p.Met710=
|
|
XM_011534150.1:c.2085G=
|
XP_011532452.1:p.Met695=
|
|
XM_011534151.1:c.2076G=
|
XP_011532453.1:p.Met692=
|
|
XM_011534152.1:c.2016G=
|
XP_011532454.1:p.Met672=
|
|
XM_011534149.3:c.2130G=
|
XP_011532451.1:p.Met710=
|
|
XM_011534150.3:c.2085G=
|
XP_011532452.1:p.Met695=
|
|
XM_011534151.3:c.2076G=
|
XP_011532453.1:p.Met692=
|
|
XM_011534152.2:c.2016G=
|
XP_011532454.1:p.Met672=
|
|
XM_017007303.2:c.2007G=
|
XP_016862792.1:p.Met669=
|
|
NM_004656.4:c.2061G=
MANE Select
|
NP_004647.1:p.Met687=
|
|