ENST00000703783.1:n.737T=
|
|
|
ENST00000703785.1:n.818T=
|
|
|
ENST00000262464.9:c.3953T=
MANE Select
|
ENSP00000262464.4:p.Met1318=
|
|
ENST00000262464.8:c.3953T=
|
ENSP00000262464.4:p.Met1318=
|
|
ENST00000507835.5:c.503T=
|
ENSP00000426839.1:p.Met168=
|
|
ENST00000508053.5:c.3953T=
|
ENSP00000424571.1:p.Met1318=
|
|
ENST00000508989.5:c.3854T=
|
ENSP00000425596.1:p.Met1285=
|
|
ENST00000619499.4:c.3950T=
|
ENSP00000482132.1:p.Met1317=
|
|
NM_001999.3:c.3953T=
|
NP_001990.2:p.Met1318=
|
|
XM_017009228.2:c.3800T=
|
XP_016864717.1:p.Met1267=
|
|
NM_001999.4:c.3953T=
MANE Select
|
NP_001990.2:p.Met1318=
|
|