ENST00000573725.2:c.6603G>T
|
ENSP00000460849.2:p.Met2201Ile
|
|
ENST00000703537.1:c.2531G>T
|
|
|
ENST00000703538.1:c.*6506G>T
|
ENSP00000515361.1:n.*6506G>T
|
|
ENST00000703539.1:n.3097G>T
|
|
|
ENST00000703540.1:c.6636G>T
|
ENSP00000515362.1:p.Met2212Ile
|
|
ENST00000703541.1:c.6648G>T
|
ENSP00000515363.1:p.Met2216Ile
|
|
ENST00000304992.11:c.6783G>T
MANE Select
|
ENSP00000304350.6:p.Met2261Ile
|
|
ENST00000304992.10:c.6783G>T
|
ENSP00000304350.6:p.Met2261Ile
|
|
ENST00000571958.1:c.92G>T
|
|
|
ENST00000572621.5:c.6783G>T
|
ENSP00000460348.1:p.Met2261Ile
|
|
ENST00000572723.1:n.772G>T
|
|
|
NM_006445.3:c.6783G>T
|
NP_006436.3:p.Met2261Ile
|
|
XM_024450537.1:c.6783G>T
|
XP_024306305.1:p.Met2261Ile
|
|
NM_006445.4:c.6783G>T
MANE Select
|
NP_006436.3:p.Met2261Ile
|
|