ENST00000352909.8:c.973G>A
MANE Select
|
ENSP00000325951.4:p.Glu325Lys
|
|
ENST00000324155.8:c.*662G>A
|
ENSP00000325831.3:n.*662G>A
|
|
ENST00000333684.9:c.696-88G>A
|
ENSP00000328814.6:n.696-88G>A
|
|
ENST00000352909.7:c.973G>A
|
ENSP00000325951.3:p.Glu325Lys
|
|
ENST00000381168.7:c.*693G>A
|
ENSP00000370560.3:n.*693G>A
|
|
ENST00000381175.5:c.1054G>A
|
ENSP00000370567.1:p.Glu352Lys
|
|
ENST00000381178.5:c.1066G>A
|
ENSP00000370571.1:p.Glu356Lys
|
|
ENST00000412076.1:c.136-88G>A
|
|
|
ENST00000416223.5:c.267G>A
|
|
|
ENST00000461172.1:n.138G>A
|
|
|
ENST00000479437.5:n.522G>A
|
|
|
NM_000360.3:c.973G>A
|
NP_000351.2:p.Glu325Lys
|
|
NM_199292.2:c.1066G>A
|
NP_954986.2:p.Glu356Lys
|
|
NM_199293.2:c.1054G>A
|
NP_954987.2:p.Glu352Lys
|
|
XM_011520335.1:c.985G>A
|
XP_011518637.1:p.Glu329Lys
|
|
XM_011520335.2:c.985G>A
|
XP_011518637.1:p.Glu329Lys
|
|
NM_000360.4:c.973G>A
MANE Select
|
NP_000351.2:p.Glu325Lys
|
|
NM_199292.3:c.1066G>A
|
NP_954986.2:p.Glu356Lys
|
|
NM_199293.3:c.1054G>A
|
NP_954987.2:p.Glu352Lys
|
|