ENST00000227665.9:c.258A>T
MANE Select
|
ENSP00000227665.4:p.Pro86=
|
|
ENST00000433069.2:c.258A>T
|
ENSP00000399701.2:p.Pro86=
|
|
ENST00000673688.1:c.342A>T
|
ENSP00000501141.1:p.Pro114=
|
|
ENST00000227665.8:c.258A>T
|
ENSP00000227665.4:p.Pro86=
|
|
ENST00000433069.1:c.258A>T
|
ENSP00000399701.1:p.Pro86=
|
|
ENST00000542499.5:c.258A>T
|
ENSP00000445002.1:p.Pro86=
|
|
NM_001166598.1:c.258A>T
|
NP_001160070.1:p.Pro86=
|
|
NM_052968.4:c.258A>T
|
NP_443200.2:p.Pro86=
|
|
NM_001166598.2:c.258A>T
|
NP_001160070.1:p.Pro86=
|
|
NM_001371904.1:c.258A>T
MANE Select
|
NP_001358833.1:p.Pro86=
|
|
NM_052968.5:c.258A>T
|
NP_443200.2:p.Pro86=
|
|