ENST00000496887.7:c.1280C>G
|
ENSP00000434560.2:p.Ser427Trp
|
|
ENST00000646564.2:c.1097C>G
|
ENSP00000495806.2:p.Ser366Trp
|
|
ENST00000155840.12:c.1637C>G
MANE Select
|
ENSP00000155840.2:p.Ser546Trp
|
|
ENST00000335475.6:c.1256C>G
|
ENSP00000334497.5:p.Ser419Trp
|
|
ENST00000646564.1:c.743C>G
|
ENSP00000495806.1:p.Ser248Trp
|
|
ENST00000155840.9:c.1637C>G
|
ENSP00000155840.2:p.Ser546Trp
|
|
ENST00000335475.5:c.1256C>G
|
ENSP00000334497.5:p.Ser419Trp
|
|
NM_000218.2:c.1637C>G , LRG_287t1:c.1637C>G
|
NP_000209.2:p.Ser546Trp
|
|
NM_181798.1:c.1256C>G , LRG_287t2:c.1256C>G
|
NP_861463.1:p.Ser419Trp
|
|
NM_000218.3:c.1637C>G
MANE Select
|
NP_000209.2:p.Ser546Trp
|
|