ENST00000344265.8:c.795T>G
|
ENSP00000342931.3:p.Pro265=
|
|
ENST00000350375.7:c.717T>G
MANE Select
|
ENSP00000263781.2:p.Pro239=
|
|
ENST00000344265.7:c.795T>G
|
ENSP00000342931.3:p.Pro265=
|
|
ENST00000350375.6:c.717T>G
|
ENSP00000263781.2:p.Pro239=
|
|
ENST00000560656.1:c.491T>G
|
ENSP00000452610.1:p.Leu164Arg
|
|
ENST00000561167.5:c.492T>G
|
ENSP00000454072.1:p.Pro164=
|
|
NM_000306.3:c.717T>G
|
NP_000297.1:p.Pro239=
|
|
NM_001122757.2:c.795T>G
|
NP_001116229.1:p.Pro265=
|
|
NM_000306.4:c.717T>G
MANE Select
|
NP_000297.1:p.Pro239=
|
|
NM_001122757.3:c.795T>G
|
NP_001116229.1:p.Pro265=
|
|