ENST00000280551.11:c.603T>G
MANE Select
|
ENSP00000280551.6:p.Pro201=
|
|
ENST00000280551.10:c.603T>G
|
ENSP00000280551.6:p.Pro201=
|
|
ENST00000419654.6:c.-730T>G
|
ENSP00000388324.2:n.-730T>G
|
|
ENST00000506622.5:c.710T>G
|
ENSP00000427249.1:p.Leu237Arg
|
|
ENST00000509818.5:c.454T>G
|
ENSP00000424085.1:p.Ser152Ala
|
|
ENST00000514561.5:c.*577T>G
|
ENSP00000422717.1:n.*577T>G
|
|
NM_014822.2:c.603T>G
|
NP_055637.2:p.Pro201=
|
|
XM_005263378.1:c.603T>G
|
XP_005263435.1:p.Pro201=
|
|
XM_005263379.1:c.603T>G
|
XP_005263436.1:p.Pro201=
|
|
XM_011532435.1:c.603T>G
|
XP_011530737.1:p.Pro201=
|
|
XM_011532436.1:c.603T>G
|
XP_011530738.1:p.Pro201=
|
|
NM_001318066.1:c.603T>G
|
NP_001304995.1:p.Pro201=
|
|
NM_014822.3:c.603T>G
|
NP_055637.2:p.Pro201=
|
|
XM_005263379.3:c.603T>G
|
XP_005263436.1:p.Pro201=
|
|
XM_024454293.1:c.603T>G
|
XP_024310061.1:p.Pro201=
|
|
NM_014822.4:c.603T>G
MANE Select
|
NP_055637.2:p.Pro201=
|
|
NM_001318066.2:c.603T>G
|
NP_001304995.1:p.Pro201=
|
|