|
ENST00000233202.11:c.212C>G
MANE Select
|
ENSP00000233202.6:p.Ala71Gly
|
|
|
ENST00000233202.10:c.212C>G
|
ENSP00000233202.6:p.Ala71Gly
|
|
|
ENST00000354352.9:c.212C>G
|
ENSP00000346320.5:p.Ala71Gly
|
|
|
ENST00000465984.5:n.332-843C>G
|
|
|
|
ENST00000468221.5:n.1692C>G
|
|
|
|
ENST00000469449.1:n.618C>G
|
|
|
|
ENST00000469799.5:n.98-843C>G
|
|
|
|
ENST00000471875.5:n.159C>G
|
|
|
|
ENST00000473367.5:c.151-15C>G
|
ENSP00000484905.1:n.151-15C>G
|
|
|
ENST00000475225.5:n.186-15C>G
|
|
|
|
ENST00000481524.5:c.8-843C>G
|
ENSP00000483970.1:n.8-843C>G
|
|
|
ENST00000483487.2:n.138C>G
|
|
|
|
ENST00000492413.5:n.294C>G
|
|
|
|
ENST00000494322.5:n.308C>G
|
|
|
|
ENST00000539932.5:c.69C>G
|
ENSP00000443435.2:p.Cys23Trp
|
|
|
NM_000578.3:c.212C>G
|
NP_000569.3:p.Ala71Gly
|
|
|
XM_005246793.2:c.11C>G
|
XP_005246850.1:p.Ala4Gly
|
|
|
XM_005246794.2:c.-217C>G
|
XP_005246851.1:n.-217C>G
|
|
|
XM_006712709.2:c.-217C>G
|
XP_006712772.1:n.-217C>G
|
|
|
XM_006712710.2:c.-155-843C>G
|
XP_006712773.1:n.-155-843C>G
|
|
|
XM_006712711.2:c.-174-843C>G
|
XP_006712774.1:n.-174-843C>G
|
|
|
XM_011511684.1:c.-225C>G
|
XP_011509986.1:n.-225C>G
|
|
|
XM_011511685.1:c.-225C>G
|
XP_011509987.1:n.-225C>G
|
|
|
XR_427107.1:n.375C>G
|
|
|
|
XR_427108.2:n.672C>G
|
|
|
|
XM_005246793.4:c.11C>G
|
XP_005246850.1:p.Ala4Gly
|
|
|
XM_005246794.4:c.-217C>G
|
XP_005246851.1:n.-217C>G
|
|
|
XM_006712709.4:c.-217C>G
|
XP_006712772.1:n.-217C>G
|
|
|
XM_006712710.4:c.-155-843C>G
|
XP_006712773.1:n.-155-843C>G
|
|
|
XM_006712711.4:c.-174-843C>G
|
XP_006712774.1:n.-174-843C>G
|
|
|
XM_011511684.3:c.-225C>G
|
XP_011509986.1:n.-225C>G
|
|
|
XM_011511685.3:c.-225C>G
|
XP_011509987.1:n.-225C>G
|
|
|
XM_017004765.2:c.151-843C>G
|
XP_016860254.1:n.151-843C>G
|
|
|
XM_017004766.2:c.11C>G
|
XP_016860255.1:p.Ala4Gly
|
|
|
XM_017004767.2:c.212C>G
|
XP_016860256.1:p.Ala71Gly
|
|
|
XR_427107.3:n.361C>G
|
|
|
|
XR_427108.4:n.672C>G
|
|
|
|
NM_000578.4:c.212C>G
MANE Select
|
NP_000569.3:p.Ala71Gly
|
|
