ENST00000496887.7:c.828C>G
|
ENSP00000434560.2:p.Tyr276Ter
|
|
ENST00000646564.2:c.645C>G
|
ENSP00000495806.2:p.Tyr215Ter
|
|
ENST00000155840.12:c.1185C>G
MANE Select
|
ENSP00000155840.2:p.Tyr395Ter
|
|
ENST00000335475.6:c.804C>G
|
ENSP00000334497.5:p.Tyr268Ter
|
|
ENST00000646564.1:c.291C>G
|
ENSP00000495806.1:p.Tyr97Ter
|
|
ENST00000155840.9:c.1185C>G
|
ENSP00000155840.2:p.Tyr395Ter
|
|
ENST00000335475.5:c.804C>G
|
ENSP00000334497.5:p.Tyr268Ter
|
|
NM_000218.2:c.1185C>G , LRG_287t1:c.1185C>G
|
NP_000209.2:p.Tyr395Ter
|
|
NM_181798.1:c.804C>G , LRG_287t2:c.804C>G
|
NP_861463.1:p.Tyr268Ter
|
|
NM_000218.3:c.1185C>G
MANE Select
|
NP_000209.2:p.Tyr395Ter
|
|