ENST00000496887.7:c.1426G=
|
ENSP00000434560.2:p.Val476=
|
|
ENST00000646564.2:c.1243G=
|
ENSP00000495806.2:p.Val415=
|
|
ENST00000155840.12:c.1783G=
MANE Select
|
ENSP00000155840.2:p.Val595=
|
|
ENST00000335475.6:c.1402G=
|
ENSP00000334497.5:p.Val468=
|
|
ENST00000526095.2:c.187G=
|
ENSP00000494939.1:p.Val63=
|
|
ENST00000646564.1:c.889G=
|
ENSP00000495806.1:p.Val297=
|
|
ENST00000155840.9:c.1783G=
|
ENSP00000155840.2:p.Val595=
|
|
ENST00000335475.5:c.1402G=
|
ENSP00000334497.5:p.Val468=
|
|
ENST00000526095.1:n.290G=
|
|
|
NM_000218.2:c.1783G= , LRG_287t1:c.1783G=
|
NP_000209.2:p.Val595=
|
|
NM_181798.1:c.1402G= , LRG_287t2:c.1402G=
|
NP_861463.1:p.Val468=
|
|
NM_000218.3:c.1783G=
MANE Select
|
NP_000209.2:p.Val595=
|
|