ENST00000496887.7:c.1185T>G
|
ENSP00000434560.2:p.Ile395Met
|
|
ENST00000646564.2:c.1002T>G
|
ENSP00000495806.2:p.Ile334Met
|
|
ENST00000155840.12:c.1542T>G
MANE Select
|
ENSP00000155840.2:p.Ile514Met
|
|
ENST00000335475.6:c.1161T>G
|
ENSP00000334497.5:p.Ile387Met
|
|
ENST00000646564.1:c.648T>G
|
ENSP00000495806.1:p.Ile216Met
|
|
ENST00000155840.9:c.1542T>G
|
ENSP00000155840.2:p.Ile514Met
|
|
ENST00000335475.5:c.1161T>G
|
ENSP00000334497.5:p.Ile387Met
|
|
NM_000218.2:c.1542T>G , LRG_287t1:c.1542T>G
|
NP_000209.2:p.Ile514Met
|
|
NM_181798.1:c.1161T>G , LRG_287t2:c.1161T>G
|
NP_861463.1:p.Ile387Met
|
|
NM_000218.3:c.1542T>G
MANE Select
|
NP_000209.2:p.Ile514Met
|
|