ENST00000294288.5:c.291C>G
MANE Select
|
ENSP00000294288.4:p.Tyr97Ter
|
|
ENST00000545205.2:c.*76C>G
|
ENSP00000446180.1:n.*76C>G
|
|
ENST00000636477.1:c.243C>G
|
ENSP00000490746.1:p.Tyr81Ter
|
|
ENST00000294288.4:c.291C>G
|
ENSP00000294288.4:p.Tyr97Ter
|
|
ENST00000353903.9:c.120C>G
|
ENSP00000312037.4:p.Tyr40Ter
|
|
ENST00000545205.1:c.*76C>G
|
ENSP00000446180.1:n.*76C>G
|
|
NM_016366.2:c.291C>G
|
NP_057450.2:p.Tyr97Ter
|
|
XM_005274046.1:c.309C>G
|
XP_005274103.1:p.Tyr103Ter
|
|
NM_001318496.1:c.309C>G
|
NP_001305425.1:p.Tyr103Ter
|
|
NM_001318496.2:c.309C>G
|
NP_001305425.1:p.Tyr103Ter
|
|
NM_016366.3:c.291C>G
MANE Select
|
NP_057450.2:p.Tyr97Ter
|
|