ENST00000294288.5:c.339G>T
MANE Select
|
ENSP00000294288.4:p.Met113Ile
|
|
ENST00000545205.2:c.*124G>T
|
ENSP00000446180.1:n.*124G>T
|
|
ENST00000636477.1:c.291G>T
|
ENSP00000490746.1:p.Met97Ile
|
|
ENST00000294288.4:c.339G>T
|
ENSP00000294288.4:p.Met113Ile
|
|
ENST00000353903.9:c.168G>T
|
ENSP00000312037.4:p.Met56Ile
|
|
ENST00000545205.1:c.*124G>T
|
ENSP00000446180.1:n.*124G>T
|
|
NM_016366.2:c.339G>T
|
NP_057450.2:p.Met113Ile
|
|
XM_005274046.1:c.357G>T
|
XP_005274103.1:p.Met119Ile
|
|
NM_001318496.1:c.357G>T
|
NP_001305425.1:p.Met119Ile
|
|
NM_001318496.2:c.357G>T
|
NP_001305425.1:p.Met119Ile
|
|
NM_016366.3:c.339G>T
MANE Select
|
NP_057450.2:p.Met113Ile
|
|