ENST00000496887.7:c.482G>A
|
ENSP00000434560.2:p.Trp161Ter
|
|
ENST00000646564.2:c.478-11363G>A
|
ENSP00000495806.2:n.478-11363G>A
|
|
ENST00000155840.12:c.743G>A
MANE Select
|
ENSP00000155840.2:p.Trp248Ter
|
|
ENST00000335475.6:c.362G>A
|
ENSP00000334497.5:p.Trp121Ter
|
|
ENST00000646564.1:c.124-11363G>A
|
ENSP00000495806.1:n.124-11363G>A
|
|
ENST00000155840.9:c.743G>A
|
ENSP00000155840.2:p.Trp248Ter
|
|
ENST00000335475.5:c.362G>A
|
ENSP00000334497.5:p.Trp121Ter
|
|
ENST00000496887.6:c.482G>A
|
ENSP00000434560.1:p.Trp161Ter
|
|
NM_000218.2:c.743G>A , LRG_287t1:c.743G>A
|
NP_000209.2:p.Trp248Ter
|
|
NM_181798.1:c.362G>A , LRG_287t2:c.362G>A
|
NP_861463.1:p.Trp121Ter
|
|
NM_000218.3:c.743G>A
MANE Select
|
NP_000209.2:p.Trp248Ter
|
|