ENST00000227665.9:c.909C>T
MANE Select
|
ENSP00000227665.4:p.Ile303=
|
|
ENST00000433069.2:c.909C>T
|
ENSP00000399701.2:p.Ile303=
|
|
ENST00000673688.1:c.993C>T
|
ENSP00000501141.1:p.Ile331=
|
|
ENST00000227665.8:c.909C>T
|
ENSP00000227665.4:p.Ile303=
|
|
ENST00000542499.5:c.909C>T
|
ENSP00000445002.1:p.Ile303=
|
|
NM_001166598.1:c.909C>T
|
NP_001160070.1:p.Ile303=
|
|
NM_052968.4:c.909C>T
|
NP_443200.2:p.Ile303=
|
|
NM_001166598.2:c.909C>T
|
NP_001160070.1:p.Ile303=
|
|
NM_001371904.1:c.909C>T
MANE Select
|
NP_001358833.1:p.Ile303=
|
|
NM_052968.5:c.909C>T
|
NP_443200.2:p.Ile303=
|
|