ENST00000642496.1:c.3961T=
|
|
|
ENST00000644397.2:c.5102T=
MANE Select
|
ENSP00000495195.1:p.Met1701=
|
|
ENST00000373965.6:c.4913T=
|
ENSP00000363076.3:p.Met1638=
|
|
ENST00000414778.5:c.4910T=
|
ENSP00000410304.2:p.Met1637=
|
|
ENST00000495484.5:c.1130T=
|
ENSP00000480780.1:p.Met377=
|
|
ENST00000614895.4:c.4925T=
|
ENSP00000478512.1:p.Met1642=
|
|
ENST00000616114.4:c.4907T=
|
ENSP00000483745.1:p.Met1636=
|
|
ENST00000618301.4:c.1262T=
|
ENSP00000482780.1:p.Met421=
|
|
ENST00000621708.4:c.4928T=
|
ENSP00000484454.1:p.Met1643=
|
|
NM_001142771.1:c.4928T=
|
NP_001136243.1:p.Met1643=
|
|
NM_001142772.1:c.4913T=
|
NP_001136244.1:p.Met1638=
|
|
NM_001354420.1:c.4907T=
|
NP_001341349.1:p.Met1636=
|
|
NM_001354429.1:c.5036T=
|
NP_001341358.1:p.Met1679=
|
|
XR_001747192.2:n.11394T=
|
|
|
XR_001747193.2:n.11385T=
|
|
|
NM_001142771.2:c.4928T=
|
NP_001136243.1:p.Met1643=
|
|
NM_001142772.2:c.4913T=
|
NP_001136244.1:p.Met1638=
|
|
NM_001354420.2:c.4907T=
|
NP_001341349.1:p.Met1636=
|
|
NM_001354429.2:c.5036T=
|
NP_001341358.1:p.Met1679=
|
|
NM_001384140.1:c.5102T=
MANE Select
|
NP_001371069.1:p.Met1701=
|
|